Linked Data
dbSNP Id:
rs782215521
ExAC:
13:115090332 CCTG / C
gnomAD v2:
13-115090332-CCTG-C
gnomAD v3:
13-114324857-CCTG-C
gnomAD v4:
13-114324857-CCTG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.114324860_114324862del , CM000675.2:g.114324860_114324862del | GRCh38 |
| NC_000013.10:g.115090335_115090337del , CM000675.1:g.115090335_115090337del | GRCh37 |
| NC_000013.9:g.114108437_114108439del | NCBI36 |
| NG_051829.1:g.15526_15528del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643483.2:c.1018_1020del | ENSP00000496699.1:p.Ala340del | |
| ENST00000644294.2:c.1018_1020del | ENSP00000495985.2:p.Ala340del | |
| ENST00000645174.2:c.1018_1020del | ENSP00000494031.2:p.Ala340del | |
| ENST00000700527.1:c.1018_1020del | ENSP00000515032.1:p.Ala340del | |
| ENST00000700528.1:c.1018_1020del | ENSP00000515033.1:p.Ala340del | |
| ENST00000361283.4:c.1018_1020del MANE Select | ENSP00000354730.1:p.Ala340del | |
| ENST00000643483.1:c.1018_1020del | ENSP00000496699.1:p.Ala340del | |
| ENST00000646155.1:n.123+10217_123+10219del | ||
| ENST00000646956.1:n.285+3628_285+3630del | ||
| ENST00000361283.2:c.1018_1020del | ENSP00000354730.1:p.Ala340del | |
| NM_001164144.1:c.1018_1020del | NP_001157616.1:p.Ala340del | |
| NM_001164145.1:c.1018_1020del | NP_001157617.1:p.Ala340del | |
| NM_032436.2:c.1018_1020del | NP_115812.1:p.Ala340del | |
| NM_001164144.2:c.1018_1020del | NP_001157616.1:p.Ala340del | |
| NM_001164145.2:c.1018_1020del | NP_001157617.1:p.Ala340del | |
| NM_032436.3:c.1018_1020del | NP_115812.1:p.Ala340del | |
| NM_032436.4:c.1018_1020del MANE Select | NP_115812.1:p.Ala340del | |
| NM_001164144.3:c.1018_1020del | NP_001157616.1:p.Ala340del | |
| NM_001164145.3:c.1018_1020del | NP_001157617.1:p.Ala340del |