Canonical Allele Identifier: CA2844096572
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271124_31271125dup , CM000668.2:g.31271124_31271125dup GRCh38
NC_000006.11:g.31238901_31238902dup , CM000668.1:g.31238901_31238902dup GRCh37
NC_000006.10:g.31346880_31346881dup NCBI36
NG_029422.2:g.6007_6008dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.567_568dup MANE Select ENSP00000365402.5:p.Glu190GlyfsTer25
ENST00000376228.9:c.567_568dup ENSP00000365402.5:p.Glu190GlyfsTer25
ENST00000376237.8:c.*154_*155dup ENSP00000365412.4:n.*154_*155dup
ENST00000383329.7:c.567_568dup ENSP00000372819.3:p.Glu190GlyfsTer25
ENST00000415537.1:c.565_566dup
ENST00000484378.1:n.836_837dup
ENST00000487245.5:n.926_927dup
ENST00000495835.1:n.756_757dup
NM_002117.5:c.567_568dup NP_002108.4:p.Glu190GlyfsTer25
NM_002117.6:c.567_568dup MANE Select NP_002108.4:p.Glu190GlyfsTer25