Canonical Allele Identifier: CA1619080326
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271121_31271122delinsAC , CM000668.2:g.31271121_31271122delinsAC GRCh38
NC_000006.11:g.31238898_31238899delinsAC , CM000668.1:g.31238898_31238899delinsAC GRCh37
NC_000006.10:g.31346877_31346878delinsAC NCBI36
NG_029422.2:g.6010_6011delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.570_571delinsGT MANE Select ENSP00000365402.5:p.Glu190=
ENST00000376228.9:c.570_571delinsGT ENSP00000365402.5:p.Glu190=
ENST00000376237.8:c.*157_*158delinsGT ENSP00000365412.4:n.*157_*158delinsGT
ENST00000383329.7:c.570_571delinsGT ENSP00000372819.3:p.Glu190=
ENST00000415537.1:c.568_569delinsGT
ENST00000484378.1:n.839_840delinsGT
ENST00000487245.5:n.929_930delinsGT
ENST00000495835.1:n.759_760delinsGT
NM_002117.5:c.570_571delinsGT NP_002108.4:p.Glu190=
NM_002117.6:c.570_571delinsGT MANE Select NP_002108.4:p.Glu190=