Canonical Allele Identifier: CA1619080324
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271120C= , CM000668.2:g.31271120C= GRCh38
NC_000006.11:g.31238897C= , CM000668.1:g.31238897C= GRCh37
NC_000006.10:g.31346876C= NCBI36
NG_029422.2:g.6012G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.572G= MANE Select ENSP00000365402.5:p.Trp191=
ENST00000376228.9:c.572G= ENSP00000365402.5:p.Trp191=
ENST00000376237.8:c.*159G= ENSP00000365412.4:n.*159G=
ENST00000383329.7:c.572G= ENSP00000372819.3:p.Trp191=
ENST00000415537.1:c.570G=
ENST00000484378.1:n.841G=
ENST00000487245.5:n.931G=
ENST00000495835.1:n.761G=
NM_002117.5:c.572G= NP_002108.4:p.Trp191=
NM_002117.6:c.572G= MANE Select NP_002108.4:p.Trp191=