Canonical Allele Identifier: CA1619080715
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271586C= , CM000668.2:g.31271586C= GRCh38
NC_000006.11:g.31239363C= , CM000668.1:g.31239363C= GRCh37
NC_000006.10:g.31347342C= NCBI36
NG_029422.2:g.5546G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+13G= MANE Select ENSP00000365402.5:n.343+13G=
ENST00000376228.9:c.343+13G= ENSP00000365402.5:n.343+13G=
ENST00000376237.8:c.343+13G= ENSP00000365412.4:n.343+13G=
ENST00000383329.7:c.343+13G= ENSP00000372819.3:n.343+13G=
ENST00000415537.1:c.341+13G=
ENST00000484378.1:n.375G=
ENST00000487245.5:n.465G=
ENST00000495835.1:n.532+13G=
NM_002117.5:c.343+13G= NP_002108.4:n.343+13G=
NM_002117.6:c.343+13G= MANE Select NP_002108.4:n.343+13G=