Canonical Allele Identifier: CA2677950303
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270016_31270024dup , CM000668.2:g.31270016_31270024dup GRCh38
NC_000006.11:g.31237793_31237801dup , CM000668.1:g.31237793_31237801dup GRCh37
NC_000006.10:g.31345772_31345780dup NCBI36
NG_029422.2:g.7114_7122dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.963_971dup MANE Select ENSP00000365402.5:p.Leu324_Gly325insAlaValLeu
ENST00000376228.9:c.963_971dup ENSP00000365402.5:p.Leu324_Gly325insAlaValLeu
ENST00000376237.8:c.*550_*558dup ENSP00000365412.4:n.*550_*558dup
ENST00000383329.7:c.963_971dup ENSP00000372819.3:p.Leu324_Gly325insAlaValLeu
ENST00000470363.5:n.281_289dup
ENST00000487245.5:n.1322_1330dup
NM_002117.5:c.963_971dup NP_002108.4:p.Leu324_Gly325insAlaValLeu
NM_002117.6:c.963_971dup MANE Select NP_002108.4:p.Leu324_Gly325insAlaValLeu