Canonical Allele Identifier: CA2677950052
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269756-C-CAT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269756_31269757insAT , CM000668.2:g.31269756_31269757insAT GRCh38
NC_000006.11:g.31237533_31237534insAT , CM000668.1:g.31237533_31237534insAT GRCh37
NC_000006.10:g.31345512_31345513insAT NCBI36
NG_029422.2:g.7375_7376insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+209_1015+210insAT MANE Select ENSP00000365402.5:n.1015+209_1015+210insAT
ENST00000376228.9:c.1015+209_1015+210insAT ENSP00000365402.5:n.1015+209_1015+210insAT
ENST00000376237.8:c.*602+209_*602+210insAT ENSP00000365412.4:n.*602+209_*602+210insAT
ENST00000383329.7:c.1015+209_1015+210insAT ENSP00000372819.3:n.1015+209_1015+210insAT
ENST00000470363.5:n.542_543insAT
ENST00000487245.5:n.1374+209_1374+210insAT
NM_002117.5:c.1015+209_1015+210insAT NP_002108.4:n.1015+209_1015+210insAT
NM_002117.6:c.1015+209_1015+210insAT MANE Select NP_002108.4:n.1015+209_1015+210insAT
Search 100 bp 5'
Search 100 bp 3'