Canonical Allele Identifier: CA1619077107
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268813T= , CM000668.2:g.31268813T= GRCh38
NC_000006.11:g.31236590T= , CM000668.1:g.31236590T= GRCh37
NC_000006.10:g.31344569T= NCBI36
NG_029422.2:g.8319A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*356A= MANE Select ENSP00000365402.5:n.*356A=
ENST00000376228.9:c.*356A= ENSP00000365402.5:n.*356A=
ENST00000376237.8:c.*1044A= ENSP00000365412.4:n.*1044A=
ENST00000383329.7:c.*356A= ENSP00000372819.3:n.*356A=
ENST00000466892.5:n.690A=
ENST00000470363.5:n.1215A=
ENST00000487245.5:n.1816A=
NM_002117.5:c.*356A= NP_002108.4:n.*356A=
NM_002117.6:c.*356A= MANE Select NP_002108.4:n.*356A=