Canonical Allele Identifier: CA1087426519

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31271151-T-TG
• gnomAD v4: 6-31271151-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271151_31271152insG , CM000668.2:g.31271151_31271152insG	GRCh38
NC_000006.11:g.31238928_31238929insG , CM000668.1:g.31238928_31238929insG	GRCh37
NC_000006.10:g.31346907_31346908insG	NCBI36
NG_029422.2:g.5980_5981insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.540_541insC MANE Select	ENSP00000365402.5:p.Arg181GlnfsTer?
ENST00000376228.9:c.540_541insC	ENSP00000365402.5:p.Arg181GlnfsTer?
ENST00000376237.8:c.*127_*128insC	ENSP00000365412.4:n.*127_*128insC
ENST00000383329.7:c.540_541insC	ENSP00000372819.3:p.Arg181GlnfsTer?
ENST00000415537.1:c.538_539insC
ENST00000484378.1:n.809_810insC
ENST00000487245.5:n.899_900insC
ENST00000495835.1:n.729_730insC
NM_002117.5:c.540_541insC	NP_002108.4:p.Arg181GlnfsTer?
NM_002117.6:c.540_541insC MANE Select	NP_002108.4:p.Arg181GlnfsTer?