Canonical Allele Identifier: CA1619077238
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269037C= , CM000668.2:g.31269037C= GRCh38
NC_000006.11:g.31236814C= , CM000668.1:g.31236814C= GRCh37
NC_000006.10:g.31344793C= NCBI36
NG_029422.2:g.8095G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*132G= MANE Select ENSP00000365402.5:n.*132G=
ENST00000376228.9:c.*132G= ENSP00000365402.5:n.*132G=
ENST00000376237.8:c.*820G= ENSP00000365412.4:n.*820G=
ENST00000383329.7:c.*132G= ENSP00000372819.3:n.*132G=
ENST00000466892.5:n.466G=
ENST00000470363.5:n.991G=
ENST00000487245.5:n.1592G=
NM_002117.5:c.*132G= NP_002108.4:n.*132G=
NM_002117.6:c.*132G= MANE Select NP_002108.4:n.*132G=