Canonical Allele Identifier: CA1619080539

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271338_31271340delinsGGT , CM000668.2:g.31271338_31271340delinsGGT	GRCh38
NC_000006.11:g.31239115_31239117delinsGGT , CM000668.1:g.31239115_31239117delinsGGT	GRCh37
NC_000006.10:g.31347094_31347096delinsGGT	NCBI36
NG_029422.2:g.5792_5794delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.352_354delinsACC MANE Select	ENSP00000365402.5:p.Thr118=
ENST00000376228.9:c.352_354delinsACC	ENSP00000365402.5:p.Thr118=
ENST00000376237.8:c.344-9_344-7delinsACC	ENSP00000365412.4:n.344-9_344-7delinsACC
ENST00000383329.7:c.352_354delinsACC	ENSP00000372819.3:p.Thr118=
ENST00000415537.1:c.350_352delinsACC
ENST00000484378.1:n.621_623delinsACC
ENST00000487245.5:n.711_713delinsACC
ENST00000495835.1:n.541_543delinsACC
NM_002117.5:c.352_354delinsACC	NP_002108.4:p.Thr118=
NM_002117.6:c.352_354delinsACC MANE Select	NP_002108.4:p.Thr118=