Canonical Allele Identifier: CA2677951551

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271493-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271493_31271494insC , CM000668.2:g.31271493_31271494insC	GRCh38
NC_000006.11:g.31239270_31239271insC , CM000668.1:g.31239270_31239271insC	GRCh37
NC_000006.10:g.31347249_31347250insC	NCBI36
NG_029422.2:g.5638_5639insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.343+105_343+106insG MANE Select	ENSP00000365402.5:n.343+105_343+106insG
ENST00000376228.9:c.343+105_343+106insG	ENSP00000365402.5:n.343+105_343+106insG
ENST00000376237.8:c.343+105_343+106insG	ENSP00000365412.4:n.343+105_343+106insG
ENST00000383329.7:c.343+105_343+106insG	ENSP00000372819.3:n.343+105_343+106insG
ENST00000415537.1:c.341+105_341+106insG
ENST00000484378.1:n.467_468insG
ENST00000487245.5:n.557_558insG
ENST00000495835.1:n.532+105_532+106insG
NM_002117.5:c.343+105_343+106insG	NP_002108.4:n.343+105_343+106insG
NM_002117.6:c.343+105_343+106insG MANE Select	NP_002108.4:n.343+105_343+106insG