Canonical Allele Identifier: CA1619080793

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271675_31271677delinsCTG , CM000668.2:g.31271675_31271677delinsCTG	GRCh38
NC_000006.11:g.31239452_31239454delinsCTG , CM000668.1:g.31239452_31239454delinsCTG	GRCh37
NC_000006.10:g.31347431_31347433delinsCTG	NCBI36
NG_029422.2:g.5455_5457delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.265_267delinsCAG MANE Select	ENSP00000365402.5:p.Gln89=
ENST00000376228.9:c.265_267delinsCAG	ENSP00000365402.5:p.Gln89=
ENST00000376237.8:c.265_267delinsCAG	ENSP00000365412.4:p.Gln89=
ENST00000383329.7:c.265_267delinsCAG	ENSP00000372819.3:p.Gln89=
ENST00000415537.1:c.263_265delinsCAG
ENST00000484378.1:n.284_286delinsCAG
ENST00000487245.5:n.374_376delinsCAG
ENST00000495835.1:n.454_456delinsCAG
NM_002117.5:c.265_267delinsCAG	NP_002108.4:p.Gln89=
NM_002117.6:c.265_267delinsCAG MANE Select	NP_002108.4:p.Gln89=