Canonical Allele Identifier: CA1619078491
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269869G= , CM000668.2:g.31269869G= GRCh38
NC_000006.11:g.31237646G= , CM000668.1:g.31237646G= GRCh37
NC_000006.10:g.31345625G= NCBI36
NG_029422.2:g.7263C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+97C= MANE Select ENSP00000365402.5:n.1015+97C=
ENST00000376228.9:c.1015+97C= ENSP00000365402.5:n.1015+97C=
ENST00000376237.8:c.*602+97C= ENSP00000365412.4:n.*602+97C=
ENST00000383329.7:c.1015+97C= ENSP00000372819.3:n.1015+97C=
ENST00000470363.5:n.430C=
ENST00000487245.5:n.1374+97C=
NM_002117.5:c.1015+97C= NP_002108.4:n.1015+97C=
NM_002117.6:c.1015+97C= MANE Select NP_002108.4:n.1015+97C=