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.
Linked Data
ClinVar Variation Id:
29626
ClinVar RCV Id:
RCV000022466
dbSNP Id:
rs587776862
MyVariant Identifiers:
chr1:g.240071924_240071935delinsT (hg19)
chr1:g.239908624_239908635delinsT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.239908624_239908635delinsT , CM000663.2:g.239908624_239908635delinsT | GRCh38 |
| NC_000001.10:g.240071924_240071935delinsT , CM000663.1:g.240071924_240071935delinsT | GRCh37 |
| NC_000001.9:g.238138547_238138558delinsT | NCBI36 |
| NG_032046.1:g.284552_284563delinsT | |
| NG_032046.2:g.526695_526706delinsT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000615928.5:c.1173_1184delinsT | ENSP00000482377.1:p.Pro392AlafsTer? | |
| ENST00000675184.1:c.1173_1184delinsT | ENSP00000502349.1:p.Pro392AlafsTer? | |
| ENST00000676153.1:c.1173_1184delinsT MANE Select | ENSP00000502667.1:p.Pro392AlafsTer? | |
| ENST00000676433.1:c.1173_1184delinsT | ENSP00000502013.1:p.Pro392AlafsTer? | |
| ENST00000255380.8:c.1173_1184delinsT | ENSP00000255380.4:p.Pro392AlafsTer? | |
| ENST00000615928.4:c.1173_1184delinsT | ENSP00000482377.1:p.Pro392AlafsTer? | |
| NM_000740.2:c.1173_1184delinsT | NP_000731.1:p.Pro392AlafsTer? | |
| XM_005273032.2:c.1173_1184delinsT | XP_005273089.1:p.Pro392AlafsTer? | |
| XM_005273034.2:c.1173_1184delinsT | XP_005273091.1:p.Pro392AlafsTer? | |
| XM_011544041.1:c.1173_1184delinsT | XP_011542343.1:p.Pro392AlafsTer? | |
| XM_011544042.1:c.1173_1184delinsT | XP_011542344.1:p.Pro392AlafsTer? | |
| XM_011544043.1:c.1173_1184delinsT | XP_011542345.1:p.Pro392AlafsTer? | |
| XM_011544044.1:c.1173_1184delinsT | XP_011542346.1:p.Pro392AlafsTer? | |
| XM_011544045.1:c.1173_1184delinsT | XP_011542347.1:p.Pro392AlafsTer? | |
| XM_011544046.1:c.1173_1184delinsT | XP_011542348.1:p.Pro392AlafsTer? | |
| XM_011544047.1:c.1173_1184delinsT | XP_011542349.1:p.Pro392AlafsTer? | |
| NM_000740.3:c.1173_1184delinsT | NP_000731.1:p.Pro392AlafsTer? | |
| NM_001347716.1:c.1173_1184delinsT | NP_001334645.1:p.Pro392AlafsTer? | |
| XM_005273032.3:c.1173_1184delinsT | XP_005273089.1:p.Pro392AlafsTer? | |
| XM_011544041.2:c.1173_1184delinsT | XP_011542343.1:p.Pro392AlafsTer? | |
| XM_011544043.2:c.1173_1184delinsT | XP_011542345.1:p.Pro392AlafsTer? | |
| XM_011544044.2:c.1173_1184delinsT | XP_011542346.1:p.Pro392AlafsTer? | |
| XM_011544046.2:c.1173_1184delinsT | XP_011542348.1:p.Pro392AlafsTer? | |
| XM_011544047.2:c.1173_1184delinsT | XP_011542349.1:p.Pro392AlafsTer? | |
| XM_017000152.2:c.1173_1184delinsT | XP_016855641.1:p.Pro392AlafsTer? | |
| XM_017000153.1:c.1173_1184delinsT | XP_016855642.1:p.Pro392AlafsTer? | |
| XM_017000154.1:c.1173_1184delinsT | XP_016855643.1:p.Pro392AlafsTer? | |
| XM_017000155.1:c.1173_1184delinsT | XP_016855644.1:p.Pro392AlafsTer? | |
| XM_017000156.1:c.1173_1184delinsT | XP_016855645.1:p.Pro392AlafsTer? | |
| XM_017000157.2:c.1173_1184delinsT | XP_016855646.1:p.Pro392AlafsTer? | |
| XM_017000158.1:c.1173_1184delinsT | XP_016855647.1:p.Pro392AlafsTer? | |
| XM_017000159.1:c.1173_1184delinsT | XP_016855648.1:p.Pro392AlafsTer? | |
| XM_017000160.2:c.1173_1184delinsT | XP_016855649.1:p.Pro392AlafsTer? | |
| XM_017000161.1:c.1173_1184delinsT | XP_016855650.1:p.Pro392AlafsTer? | |
| XM_017000162.1:c.1173_1184delinsT | XP_016855651.1:p.Pro392AlafsTer? | |
| XM_017000163.2:c.1173_1184delinsT | XP_016855652.1:p.Pro392AlafsTer? | |
| NM_001347716.2:c.1173_1184delinsT | NP_001334645.1:p.Pro392AlafsTer? | |
| NM_001375978.1:c.1173_1184delinsT MANE Select | NP_001362907.1:p.Pro392AlafsTer? | |
| NM_001375979.1:c.1173_1184delinsT | NP_001362908.1:p.Pro392AlafsTer? | |
| NM_001375980.1:c.1173_1184delinsT | NP_001362909.1:p.Pro392AlafsTer? | |
| NM_001375981.1:c.1173_1184delinsT | NP_001362910.1:p.Pro392AlafsTer? | |
| NM_001375982.1:c.1173_1184delinsT | NP_001362911.1:p.Pro392AlafsTer? | |
| NM_001375983.1:c.1173_1184delinsT | NP_001362912.1:p.Pro392AlafsTer? | |
| NM_001375984.1:c.1173_1184delinsT | NP_001362913.1:p.Pro392AlafsTer? | |
| NM_001375985.1:c.1173_1184delinsT | NP_001362914.1:p.Pro392AlafsTer? | |
| NM_000740.4:c.1173_1184delinsT | NP_000731.1:p.Pro392AlafsTer? |