Canonical Allele Identifier: CA1619080362
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271151_31271153delinsTCA , CM000668.2:g.31271151_31271153delinsTCA GRCh38
NC_000006.11:g.31238928_31238930delinsTCA , CM000668.1:g.31238928_31238930delinsTCA GRCh37
NC_000006.10:g.31346907_31346909delinsTCA NCBI36
NG_029422.2:g.5979_5981delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.539_541delinsTGA MANE Select ENSP00000365402.5:p.Leu180=
ENST00000376228.9:c.539_541delinsTGA ENSP00000365402.5:p.Leu180=
ENST00000376237.8:c.*126_*128delinsTGA ENSP00000365412.4:n.*126_*128delinsTGA
ENST00000383329.7:c.539_541delinsTGA ENSP00000372819.3:p.Leu180=
ENST00000415537.1:c.537_539delinsTGA
ENST00000484378.1:n.808_810delinsTGA
ENST00000487245.5:n.898_900delinsTGA
ENST00000495835.1:n.728_730delinsTGA
NM_002117.5:c.539_541delinsTGA NP_002108.4:p.Leu180=
NM_002117.6:c.539_541delinsTGA MANE Select NP_002108.4:p.Leu180=