Canonical Allele Identifier: CA136866558

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271132_31271133delinsC , CM000668.2:g.31271132_31271133delinsC	GRCh38
NC_000006.11:g.31238909_31238910delinsC , CM000668.1:g.31238909_31238910delinsC	GRCh37
NC_000006.10:g.31346888_31346889delinsC	NCBI36
NG_029422.2:g.5999_6000delinsG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.559_560delinsG MANE Select	ENSP00000365402.5:p.Thr187GlyfsTer27
ENST00000376228.9:c.559_560delinsG	ENSP00000365402.5:p.Thr187GlyfsTer27
ENST00000376237.8:c.*146_*147delinsG	ENSP00000365412.4:n.*146_*147delinsG
ENST00000383329.7:c.559_560delinsG	ENSP00000372819.3:p.Thr187GlyfsTer27
ENST00000415537.1:c.557_558delinsG
ENST00000484378.1:n.828_829delinsG
ENST00000487245.5:n.918_919delinsG
ENST00000495835.1:n.748_749delinsG
NM_002117.5:c.559_560delinsG	NP_002108.4:p.Thr187GlyfsTer27
NM_002117.6:c.559_560delinsG MANE Select	NP_002108.4:p.Thr187GlyfsTer27