Canonical Allele Identifier: CA1087452064
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761153923
gnomAD v3: 6-31269872-C-CA
gnomAD v4: 6-31269872-C-CA
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269872_31269873insA , CM000668.2:g.31269872_31269873insA GRCh38
NC_000006.11:g.31237649_31237650insA , CM000668.1:g.31237649_31237650insA GRCh37
NC_000006.10:g.31345628_31345629insA NCBI36
NG_029422.2:g.7259_7260insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+93_1015+94insT MANE Select ENSP00000365402.5:n.1015+93_1015+94insT
ENST00000376228.9:c.1015+93_1015+94insT ENSP00000365402.5:n.1015+93_1015+94insT
ENST00000376237.8:c.*602+93_*602+94insT ENSP00000365412.4:n.*602+93_*602+94insT
ENST00000383329.7:c.1015+93_1015+94insT ENSP00000372819.3:n.1015+93_1015+94insT
ENST00000470363.5:n.426_427insT
ENST00000487245.5:n.1374+93_1374+94insT
NM_002117.5:c.1015+93_1015+94insT NP_002108.4:n.1015+93_1015+94insT
NM_002117.6:c.1015+93_1015+94insT MANE Select NP_002108.4:n.1015+93_1015+94insT
Search 100 bp 5'
Search 100 bp 3'