Canonical Allele Identifier: CA1619078124
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269577G= , CM000668.2:g.31269577G= GRCh38
NC_000006.11:g.31237354G= , CM000668.1:g.31237354G= GRCh37
NC_000006.10:g.31345333G= NCBI36
NG_029422.2:g.7555C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-52C= MANE Select ENSP00000365402.5:n.1016-52C=
ENST00000376228.9:c.1016-52C= ENSP00000365402.5:n.1016-52C=
ENST00000376237.8:c.*603-52C= ENSP00000365412.4:n.*603-52C=
ENST00000383329.7:c.1016-34C= ENSP00000372819.3:n.1016-34C=
ENST00000466892.5:n.90C=
ENST00000470363.5:n.722C=
ENST00000487245.5:n.1375-52C=
NM_002117.5:c.1016-52C= NP_002108.4:n.1016-52C=
NM_002117.6:c.1016-52C= MANE Select NP_002108.4:n.1016-52C=