Canonical Allele Identifier: CA2844096553
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271255_31271256dup , CM000668.2:g.31271255_31271256dup GRCh38
NC_000006.11:g.31239032_31239033dup , CM000668.1:g.31239032_31239033dup GRCh37
NC_000006.10:g.31347011_31347012dup NCBI36
NG_029422.2:g.5876_5877dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.436_437dup MANE Select ENSP00000365402.5:p.Asp146GlufsTer6
ENST00000376228.9:c.436_437dup ENSP00000365402.5:p.Asp146GlufsTer6
ENST00000376237.8:c.*23_*24dup ENSP00000365412.4:n.*23_*24dup
ENST00000383329.7:c.436_437dup ENSP00000372819.3:p.Asp146GlufsTer6
ENST00000415537.1:c.434_435dup
ENST00000484378.1:n.705_706dup
ENST00000487245.5:n.795_796dup
ENST00000495835.1:n.625_626dup
NM_002117.5:c.436_437dup NP_002108.4:p.Asp146GlufsTer6
NM_002117.6:c.436_437dup MANE Select NP_002108.4:p.Asp146GlufsTer6