Canonical Allele Identifier: CA2677951289

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271163-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271163_31271164insA , CM000668.2:g.31271163_31271164insA	GRCh38
NC_000006.11:g.31238940_31238941insA , CM000668.1:g.31238940_31238941insA	GRCh37
NC_000006.10:g.31346919_31346920insA	NCBI36
NG_029422.2:g.5968_5969insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.528_529insT MANE Select	ENSP00000365402.5:p.Ala177CysfsTer?
ENST00000376228.9:c.528_529insT	ENSP00000365402.5:p.Ala177CysfsTer?
ENST00000376237.8:c.*115_*116insT	ENSP00000365412.4:n.*115_*116insT
ENST00000383329.7:c.528_529insT	ENSP00000372819.3:p.Ala177CysfsTer?
ENST00000415537.1:c.526_527insT
ENST00000484378.1:n.797_798insT
ENST00000487245.5:n.887_888insT
ENST00000495835.1:n.717_718insT
NM_002117.5:c.528_529insT	NP_002108.4:p.Ala177CysfsTer?
NM_002117.6:c.528_529insT MANE Select	NP_002108.4:p.Ala177CysfsTer?