Canonical Allele Identifier: CA1619080364
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271153A= , CM000668.2:g.31271153A= GRCh38
NC_000006.11:g.31238930A= , CM000668.1:g.31238930A= GRCh37
NC_000006.10:g.31346909A= NCBI36
NG_029422.2:g.5979T=

Transcript Alleles

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