Canonical Allele Identifier: CA1619080079
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270672A= , CM000668.2:g.31270672A= GRCh38
NC_000006.11:g.31238449A= , CM000668.1:g.31238449A= GRCh37
NC_000006.10:g.31346428A= NCBI36
NG_029422.2:g.6460T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-187T= MANE Select ENSP00000365402.5:n.620-187T=
ENST00000376228.9:c.620-187T= ENSP00000365402.5:n.620-187T=
ENST00000376237.8:c.*207-187T= ENSP00000365412.4:n.*207-187T=
ENST00000383329.7:c.620-187T= ENSP00000372819.3:n.620-187T=
ENST00000415537.1:c.618-187T=
ENST00000487245.5:n.979-187T=
ENST00000495835.1:n.809-187T=
NM_002117.5:c.620-187T= NP_002108.4:n.620-187T=
NM_002117.6:c.620-187T= MANE Select NP_002108.4:n.620-187T=