Canonical Allele Identifier: CA2677951285
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271155_31271156insAA , CM000668.2:g.31271155_31271156insAA GRCh38
NC_000006.11:g.31238932_31238933insAA , CM000668.1:g.31238932_31238933insAA GRCh37
NC_000006.10:g.31346911_31346912insAA NCBI36
NG_029422.2:g.5976_5977insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.536_537insTT MANE Select ENSP00000365402.5:p.Gln179HisfsTer3
ENST00000376228.9:c.536_537insTT ENSP00000365402.5:p.Gln179HisfsTer3
ENST00000376237.8:c.*123_*124insTT ENSP00000365412.4:n.*123_*124insTT
ENST00000383329.7:c.536_537insTT ENSP00000372819.3:p.Gln179HisfsTer3
ENST00000415537.1:c.534_535insTT
ENST00000484378.1:n.805_806insTT
ENST00000487245.5:n.895_896insTT
ENST00000495835.1:n.725_726insTT
NM_002117.5:c.536_537insTT NP_002108.4:p.Gln179HisfsTer3
NM_002117.6:c.536_537insTT MANE Select NP_002108.4:p.Gln179HisfsTer3