Canonical Allele Identifier: CA2677951243
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271129_31271132dup , CM000668.2:g.31271129_31271132dup GRCh38
NC_000006.11:g.31238906_31238909dup , CM000668.1:g.31238906_31238909dup GRCh37
NC_000006.10:g.31346885_31346888dup NCBI36
NG_029422.2:g.6004_6007dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.564_567dup MANE Select ENSP00000365402.5:p.Glu190ArgfsTer?
ENST00000376228.9:c.564_567dup ENSP00000365402.5:p.Glu190ArgfsTer?
ENST00000376237.8:c.*151_*154dup ENSP00000365412.4:n.*151_*154dup
ENST00000383329.7:c.564_567dup ENSP00000372819.3:p.Glu190ArgfsTer?
ENST00000415537.1:c.562_565dup
ENST00000484378.1:n.833_836dup
ENST00000487245.5:n.923_926dup
ENST00000495835.1:n.753_756dup
NM_002117.5:c.564_567dup NP_002108.4:p.Glu190ArgfsTer?
NM_002117.6:c.564_567dup MANE Select NP_002108.4:p.Glu190ArgfsTer?