Canonical Allele Identifier: CA2677951241
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271124-C-CGT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271124_31271125insGT , CM000668.2:g.31271124_31271125insGT GRCh38
NC_000006.11:g.31238901_31238902insGT , CM000668.1:g.31238901_31238902insGT GRCh37
NC_000006.10:g.31346880_31346881insGT NCBI36
NG_029422.2:g.6007_6008insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.567_568insAC MANE Select ENSP00000365402.5:p.Glu190ThrfsTer25
ENST00000376228.9:c.567_568insAC ENSP00000365402.5:p.Glu190ThrfsTer25
ENST00000376237.8:c.*154_*155insAC ENSP00000365412.4:n.*154_*155insAC
ENST00000383329.7:c.567_568insAC ENSP00000372819.3:p.Glu190ThrfsTer25
ENST00000415537.1:c.565_566insAC
ENST00000484378.1:n.836_837insAC
ENST00000487245.5:n.926_927insAC
ENST00000495835.1:n.756_757insAC
NM_002117.5:c.567_568insAC NP_002108.4:p.Glu190ThrfsTer25
NM_002117.6:c.567_568insAC MANE Select NP_002108.4:p.Glu190ThrfsTer25
Search 100 bp 5'
Search 100 bp 3'