Canonical Allele Identifier: CA1619078757
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270009A= , CM000668.2:g.31270009A= GRCh38
NC_000006.11:g.31237786A= , CM000668.1:g.31237786A= GRCh37
NC_000006.10:g.31345765A= NCBI36
NG_029422.2:g.7123T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.972T= MANE Select ENSP00000365402.5:p.Leu324=
ENST00000376228.9:c.972T= ENSP00000365402.5:p.Leu324=
ENST00000376237.8:c.*559T= ENSP00000365412.4:n.*559T=
ENST00000383329.7:c.972T= ENSP00000372819.3:p.Leu324=
ENST00000470363.5:n.290T=
ENST00000487245.5:n.1331T=
NM_002117.5:c.972T= NP_002108.4:p.Leu324=
NM_002117.6:c.972T= MANE Select NP_002108.4:p.Leu324=