Canonical Allele Identifier: CA1619080673
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271525A= , CM000668.2:g.31271525A= GRCh38
NC_000006.11:g.31239302A= , CM000668.1:g.31239302A= GRCh37
NC_000006.10:g.31347281A= NCBI36
NG_029422.2:g.5607T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+74T= MANE Select ENSP00000365402.5:n.343+74T=
ENST00000376228.9:c.343+74T= ENSP00000365402.5:n.343+74T=
ENST00000376237.8:c.343+74T= ENSP00000365412.4:n.343+74T=
ENST00000383329.7:c.343+74T= ENSP00000372819.3:n.343+74T=
ENST00000415537.1:c.341+74T=
ENST00000484378.1:n.436T=
ENST00000487245.5:n.526T=
ENST00000495835.1:n.532+74T=
NM_002117.5:c.343+74T= NP_002108.4:n.343+74T=
NM_002117.6:c.343+74T= MANE Select NP_002108.4:n.343+74T=