Canonical Allele Identifier: CA2677951245
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271130_31271131insT , CM000668.2:g.31271130_31271131insT GRCh38
NC_000006.11:g.31238907_31238908insT , CM000668.1:g.31238907_31238908insT GRCh37
NC_000006.10:g.31346886_31346887insT NCBI36
NG_029422.2:g.6001_6002insA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.561_562insA MANE Select ENSP00000365402.5:p.Cys188MetfsTer?
ENST00000376228.9:c.561_562insA ENSP00000365402.5:p.Cys188MetfsTer?
ENST00000376237.8:c.*148_*149insA ENSP00000365412.4:n.*148_*149insA
ENST00000383329.7:c.561_562insA ENSP00000372819.3:p.Cys188MetfsTer?
ENST00000415537.1:c.559_560insA
ENST00000484378.1:n.830_831insA
ENST00000487245.5:n.920_921insA
ENST00000495835.1:n.750_751insA
NM_002117.5:c.561_562insA NP_002108.4:p.Cys188MetfsTer?
NM_002117.6:c.561_562insA MANE Select NP_002108.4:p.Cys188MetfsTer?