Linked Data
dbSNP Id:
rs1228374230
gnomAD v2:
4-103519505-CAA-C
gnomAD v3:
4-102598348-CAA-C
gnomAD v4:
4-102598348-CAA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102598349_102598350del , CM000666.2:g.102598349_102598350del | GRCh38 |
| NC_000004.11:g.103519506_103519507del , CM000666.1:g.103519506_103519507del | GRCh37 |
| NC_000004.10:g.103738544_103738545del | NCBI36 |
| NG_050628.1:g.102021_102022del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507079.6:c.1661+688_1661+689del | ENSP00000426147.2:n.1661+688_1661+689del | |
| ENST00000509165.2:c.1637+688_1637+689del | ENSP00000423877.2:n.1637+688_1637+689del | |
| ENST00000697794.1:c.*1278+688_*1278+689del | ENSP00000513443.1:n.*1278+688_*1278+689del | |
| ENST00000697799.1:n.1134+688_1134+689del | ||
| ENST00000698233.1:n.1366+688_1366+689del | ||
| ENST00000226574.9:c.1637+688_1637+689del MANE Select | ENSP00000226574.4:n.1637+688_1637+689del | |
| ENST00000652569.1:c.1613+688_1613+689del | ||
| ENST00000652619.1:c.*164+688_*164+689del | ENSP00000499031.1:n.*164+688_*164+689del | |
| ENST00000226574.8:c.1637+688_1637+689del | ENSP00000226574.4:n.1637+688_1637+689del | |
| ENST00000394820.8:c.1634+688_1634+689del | ENSP00000378297.4:n.1634+688_1634+689del | |
| ENST00000505458.5:c.1634+688_1634+689del | ENSP00000424790.1:n.1634+688_1634+689del | |
| ENST00000600343.5:c.1094+688_1094+689del | ENSP00000469340.1:n.1094+688_1094+689del | |
| NM_001165412.1:c.1634+688_1634+689del | NP_001158884.1:n.1634+688_1634+689del | |
| NM_003998.3:c.1637+688_1637+689del | NP_003989.2:n.1637+688_1637+689del | |
| XM_011532006.1:c.1658+688_1658+689del | XP_011530308.1:n.1658+688_1658+689del | |
| XM_011532007.1:c.1634+688_1634+689del | XP_011530309.1:n.1634+688_1634+689del | |
| XM_011532008.1:c.1478+688_1478+689del | XP_011530310.1:n.1478+688_1478+689del | |
| XM_011532009.1:c.1241+688_1241+689del | XP_011530311.1:n.1241+688_1241+689del | |
| XR_939027.1:n.3977_3978del | ||
| NM_001319226.1:c.1634+688_1634+689del | NP_001306155.1:n.1634+688_1634+689del | |
| XM_011532006.2:c.1658+688_1658+689del | XP_011530308.1:n.1658+688_1658+689del | |
| XM_024454067.1:c.1661+688_1661+689del | XP_024309835.1:n.1661+688_1661+689del | |
| XM_024454068.1:c.1637+688_1637+689del | XP_024309836.1:n.1637+688_1637+689del | |
| XM_024454069.1:c.1502+688_1502+689del | XP_024309837.1:n.1502+688_1502+689del | |
| NM_003998.4:c.1637+688_1637+689del MANE Select | NP_003989.2:n.1637+688_1637+689del | |
| NM_001165412.2:c.1634+688_1634+689del | NP_001158884.1:n.1634+688_1634+689del | |
| NM_001319226.2:c.1634+688_1634+689del | NP_001306155.1:n.1634+688_1634+689del | |
| NM_001382625.1:c.1637+688_1637+689del | NP_001369554.1:n.1637+688_1637+689del | |
| NM_001382626.1:c.1637+688_1637+689del | NP_001369555.1:n.1637+688_1637+689del | |
| NM_001382627.1:c.1634+688_1634+689del | NP_001369556.1:n.1634+688_1634+689del | |
| NM_001382628.1:c.1595+688_1595+689del | NP_001369557.1:n.1595+688_1595+689del |