WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5987165C= , CM000669.2:g.5987165C= | GRCh38 |
| NC_000007.13:g.6026796C= , CM000669.1:g.6026796C= | GRCh37 |
| NC_000007.12:g.5993322C= | NCBI36 |
| NG_008466.1:g.26942G= , LRG_161:g.26942G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000699814.2:c.*996G= | ENSP00000514615.2:n.*996G= | |
| ENST00000699840.2:c.1597G= | ENSP00000514638.2:p.Asp533= | |
| ENST00000699930.2:c.1492G= | ENSP00000514695.2:p.Asp498= | |
| ENST00000406569.8:c.1600G= | ENSP00000514464.1:p.Asp534= | |
| ENST00000644110.2:c.*1194G= | ENSP00000496392.2:n.*1194G= | |
| ENST00000699752.1:c.1444G= | ENSP00000514561.1:p.Asp482= | |
| ENST00000699753.1:c.*1021G= | ENSP00000514562.1:n.*1021G= | |
| ENST00000699754.1:c.1402G= | ENSP00000514563.1:p.Asp468= | |
| ENST00000699755.1:c.*999G= | ENSP00000514564.1:n.*999G= | |
| ENST00000699756.1:c.*1187G= | ENSP00000514565.1:n.*1187G= | |
| ENST00000699757.1:c.*857G= | ENSP00000514566.1:n.*857G= | |
| ENST00000699758.1:c.*857G= | ENSP00000514567.1:n.*857G= | |
| ENST00000699759.1:n.2454G= | ||
| ENST00000699760.1:c.1282G= | ENSP00000514568.1:p.Asp428= | |
| ENST00000699761.1:c.1195G= | ENSP00000514569.1:p.Asp399= | |
| ENST00000699762.1:c.1027G= | ENSP00000514570.1:p.Asp343= | |
| ENST00000699763.1:c.*690G= | ENSP00000514571.1:n.*690G= | |
| ENST00000699764.1:c.1554-43G= | ENSP00000514572.1:n.1554-43G= | |
| ENST00000699765.1:c.*696G= | ENSP00000514573.1:n.*696G= | |
| ENST00000699766.1:c.1600G= | ENSP00000514574.1:p.Asp534= | |
| ENST00000699767.1:c.1600G= | ENSP00000514575.1:p.Asp534= | |
| ENST00000699768.1:c.1600G= | ENSP00000514576.1:p.Asp534= | |
| ENST00000699811.1:c.1195G= | ENSP00000514614.1:p.Asp399= | |
| ENST00000699813.1:n.1713G= | ||
| ENST00000699814.1:c.1223G= | ||
| ENST00000699815.1:c.*1131G= | ENSP00000514616.1:n.*1131G= | |
| ENST00000699816.1:c.*490G= | ENSP00000514617.1:n.*490G= | |
| ENST00000699817.1:c.*1194G= | ENSP00000514618.1:n.*1194G= | |
| ENST00000699818.1:c.1195G= | ENSP00000514619.1:p.Asp399= | |
| ENST00000699819.1:c.*757G= | ENSP00000514620.1:n.*757G= | |
| ENST00000699820.1:c.1144+2635G= | ENSP00000514621.1:n.1144+2635G= | |
| ENST00000699821.1:c.1195G= | ENSP00000514622.1:p.Asp399= | |
| ENST00000699822.1:c.*1052G= | ENSP00000514623.1:n.*1052G= | |
| ENST00000699823.1:c.1195G= | ENSP00000514624.1:p.Asp399= | |
| ENST00000699824.1:c.*1103G= | ENSP00000514625.1:n.*1103G= | |
| ENST00000699825.1:c.1039G= | ENSP00000514626.1:p.Asp347= | |
| ENST00000699826.1:c.*999G= | ENSP00000514627.1:n.*999G= | |
| ENST00000699827.1:c.1432G= | ENSP00000514628.1:p.Asp478= | |
| ENST00000699828.1:c.*690G= | ENSP00000514629.1:n.*690G= | |
| ENST00000699833.1:n.3372G= | ||
| ENST00000699837.1:c.1195G= | ENSP00000514635.1:p.Asp399= | |
| ENST00000699838.1:c.*1500G= | ENSP00000514636.1:n.*1500G= | |
| ENST00000699839.1:c.1786G= | ENSP00000514637.1:p.Asp596= | |
| ENST00000699916.1:c.*857G= | ENSP00000514684.1:n.*857G= | |
| ENST00000699917.1:c.*1049G= | ENSP00000514685.1:n.*1049G= | |
| ENST00000699918.1:c.*1101G= | ENSP00000514686.1:n.*1101G= | |
| ENST00000699919.1:c.*1187G= | ENSP00000514687.1:n.*1187G= | |
| ENST00000699920.1:c.*1236G= | ENSP00000514688.1:n.*1236G= | |
| ENST00000699928.1:c.989-4174G= | ENSP00000514693.1:n.989-4174G= | |
| ENST00000699929.1:c.*901G= | ENSP00000514694.1:n.*901G= | |
| ENST00000699930.1:c.1492G= | ENSP00000514695.1:p.Asp498= | |
| ENST00000699931.1:n.3028G= | ||
| ENST00000699951.1:c.*696G= | ENSP00000514706.1:n.*696G= | |
| ENST00000699952.1:c.803+10161G= | ENSP00000514707.1:n.803+10161G= | |
| ENST00000699953.1:c.*707G= | ENSP00000514708.1:n.*707G= | |
| ENST00000699954.1:c.*901G= | ENSP00000514709.1:n.*901G= | |
| ENST00000265849.12:c.1600G= MANE Select | ENSP00000265849.7:p.Asp534= | |
| ENST00000642292.1:c.1195G= | ENSP00000495524.1:p.Asp399= | |
| ENST00000642456.1:c.1195G= | ENSP00000493814.1:p.Asp399= | |
| ENST00000643595.1:c.*999G= | ENSP00000494497.1:n.*999G= | |
| ENST00000644110.1:c.1282G= | ENSP00000496392.1:p.Asp428= | |
| ENST00000265849.11:c.1600G= | ENSP00000265849.7:p.Asp534= | |
| ENST00000382321.5:c.804-4174G= | ENSP00000371758.4:n.804-4174G= | |
| ENST00000406569.7:n.1600G= | ||
| ENST00000441476.6:c.1282G= | ENSP00000392843.2:p.Asp428= | |
| ENST00000469652.1:n.63-4260G= | ||
| NM_000535.5:c.1600G= , LRG_161t1:c.1600G= | NP_000526.1:p.Asp534= | |
| NR_003085.2:n.1682G= | ||
| XM_006715742.2:c.1594G= | XP_006715805.1:p.Asp532= | |
| XM_006715744.2:c.667G= | XP_006715807.1:p.Asp223= | |
| XM_011515427.1:c.1645G= | XP_011513729.1:p.Asp549= | |
| XM_011515428.1:c.1489G= | XP_011513730.1:p.Asp497= | |
| XM_011515429.1:c.1282G= | XP_011513731.1:p.Asp428= | |
| XM_011515430.1:c.1282G= | XP_011513732.1:p.Asp428= | |
| NM_000535.6:c.1600G= | NP_000526.2:p.Asp534= | |
| NM_001322003.1:c.1195G= | NP_001308932.1:p.Asp399= | |
| NM_001322004.1:c.1195G= | NP_001308933.1:p.Asp399= | |
| NM_001322005.1:c.1195G= | NP_001308934.1:p.Asp399= | |
| NM_001322006.1:c.1444G= | NP_001308935.1:p.Asp482= | |
| NM_001322007.1:c.1282G= | NP_001308936.1:p.Asp428= | |
| NM_001322008.1:c.1282G= | NP_001308937.1:p.Asp428= | |
| NM_001322009.1:c.1195G= | NP_001308938.1:p.Asp399= | |
| NM_001322010.1:c.1039G= | NP_001308939.1:p.Asp347= | |
| NM_001322011.1:c.667G= | NP_001308940.1:p.Asp223= | |
| NM_001322012.1:c.667G= | NP_001308941.1:p.Asp223= | |
| NM_001322013.1:c.1027G= | NP_001308942.1:p.Asp343= | |
| NM_001322014.1:c.1600G= | NP_001308943.1:p.Asp534= | |
| NM_001322015.1:c.1291G= | NP_001308944.1:p.Asp431= | |
| NR_136154.1:n.1687G= | ||
| XM_006715744.4:c.667G= | XP_006715807.1:p.Asp223= | |
| XM_017012342.2:c.667G= | XP_016867831.1:p.Asp223= | |
| XM_024446800.1:c.1039G= | XP_024302568.1:p.Asp347= | |
| NM_000535.7:c.1600G= MANE Select | NP_000526.2:p.Asp534= | |
| NM_001322003.2:c.1195G= | NP_001308932.1:p.Asp399= | |
| NM_001322004.2:c.1195G= | NP_001308933.1:p.Asp399= | |
| NM_001322005.2:c.1195G= | NP_001308934.1:p.Asp399= | |
| NM_001322006.2:c.1444G= | NP_001308935.1:p.Asp482= | |
| NM_001322008.2:c.1282G= | NP_001308937.1:p.Asp428= | |
| NM_001322009.2:c.1195G= | NP_001308938.1:p.Asp399= | |
| NM_001322010.2:c.1039G= | NP_001308939.1:p.Asp347= | |
| NM_001322011.2:c.667G= | NP_001308940.1:p.Asp223= | |
| NM_001322012.2:c.667G= | NP_001308941.1:p.Asp223= | |
| NM_001322013.2:c.1027G= | NP_001308942.1:p.Asp343= | |
| NM_001322014.2:c.1600G= | NP_001308943.1:p.Asp534= | |
| NM_001322015.2:c.1291G= | NP_001308944.1:p.Asp431= | |
| NM_001322007.2:c.1282G= | NP_001308936.1:p.Asp428= |