Canonical Allele Identifier: CA1619080327
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271121_31271127delinsACTCCAC , CM000668.2:g.31271121_31271127delinsACTCCAC GRCh38
NC_000006.11:g.31238898_31238904delinsACTCCAC , CM000668.1:g.31238898_31238904delinsACTCCAC GRCh37
NC_000006.10:g.31346877_31346883delinsACTCCAC NCBI36
NG_029422.2:g.6005_6011delinsGTGGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.565_571delinsGTGGAGT MANE Select ENSP00000365402.5:p.Val189=
ENST00000376228.9:c.565_571delinsGTGGAGT ENSP00000365402.5:p.Val189=
ENST00000376237.8:c.*152_*158delinsGTGGAGT ENSP00000365412.4:n.*152_*158delinsGTGGAGT
ENST00000383329.7:c.565_571delinsGTGGAGT ENSP00000372819.3:p.Val189=
ENST00000415537.1:c.563_569delinsGTGGAGT
ENST00000484378.1:n.834_840delinsGTGGAGT
ENST00000487245.5:n.924_930delinsGTGGAGT
ENST00000495835.1:n.754_760delinsGTGGAGT
NM_002117.5:c.565_571delinsGTGGAGT NP_002108.4:p.Val189=
NM_002117.6:c.565_571delinsGTGGAGT MANE Select NP_002108.4:p.Val189=