Canonical Allele Identifier: CA1087428539
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271674_31271675insGGAGAA , CM000668.2:g.31271674_31271675insGGAGAA GRCh38
NC_000006.11:g.31239451_31239452insGGAGAA , CM000668.1:g.31239451_31239452insGGAGAA GRCh37
NC_000006.10:g.31347430_31347431insGGAGAA NCBI36
NG_029422.2:g.5457_5458insTTCTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.267_268insTTCTCC MANE Select ENSP00000365402.5:p.Gln89_Lys90insPheSer
ENST00000376228.9:c.267_268insTTCTCC ENSP00000365402.5:p.Gln89_Lys90insPheSer
ENST00000376237.8:c.267_268insTTCTCC ENSP00000365412.4:p.Gln89_Lys90insPheSer
ENST00000383329.7:c.267_268insTTCTCC ENSP00000372819.3:p.Gln89_Lys90insPheSer
ENST00000415537.1:c.265_266insTTCTCC
ENST00000484378.1:n.286_287insTTCTCC
ENST00000487245.5:n.376_377insTTCTCC
ENST00000495835.1:n.456_457insTTCTCC
NM_002117.5:c.267_268insTTCTCC NP_002108.4:p.Gln89_Lys90insPheSer
NM_002117.6:c.267_268insTTCTCC MANE Select NP_002108.4:p.Gln89_Lys90insPheSer