Canonical Allele Identifier: CA1619077364
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269138C= , CM000668.2:g.31269138C= GRCh38
NC_000006.11:g.31236915C= , CM000668.1:g.31236915C= GRCh37
NC_000006.10:g.31344894C= NCBI36
NG_029422.2:g.7994G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*31G= MANE Select ENSP00000365402.5:n.*31G=
ENST00000376228.9:c.*31G= ENSP00000365402.5:n.*31G=
ENST00000376237.8:c.*719G= ENSP00000365412.4:n.*719G=
ENST00000383329.7:c.*31G= ENSP00000372819.3:n.*31G=
ENST00000466892.5:n.365G=
ENST00000470363.5:n.890G=
ENST00000487245.5:n.1491G=
NM_002117.5:c.*31G= NP_002108.4:n.*31G=
NM_002117.6:c.*31G= MANE Select NP_002108.4:n.*31G=