Canonical Allele Identifier: CA137040391

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs35171346
• gnomAD v4: 6-33069636-C-CA
• MyVariant Identifiers: chr6:g.33037413_33037414insA (hg19) ; chr6:g.33069636_33069637insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33069636_33069637insA , CM000668.2:g.33069636_33069637insA	GRCh38
NC_000006.11:g.33037413_33037414insA , CM000668.1:g.33037413_33037414insA	GRCh37
NC_000006.10:g.33145391_33145392insA	NCBI36
NG_033241.1:g.16142_16143insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692443.1:c.346+4_346+5insT MANE Select	ENSP00000509163.1:n.346+4_346+5insT
ENST00000419277.5:c.346+4_346+5insT	ENSP00000393566.1:n.346+4_346+5insT
ENST00000453337.1:c.346+4_346+5insT	ENSP00000390929.1:n.346+4_346+5insT
ENST00000463066.1:n.441+4_441+5insT
ENST00000476642.5:n.322+4_322+5insT
ENST00000479107.1:n.395_396insT
NM_001242524.1:c.346+4_346+5insT	NP_001229453.1:n.346+4_346+5insT
NM_001242525.1:c.346+4_346+5insT	NP_001229454.1:n.346+4_346+5insT
NM_033554.3:c.346+4_346+5insT	NP_291032.2:n.346+4_346+5insT
XM_011514559.1:c.346+4_346+5insT	XP_011512861.1:n.346+4_346+5insT
NM_001242524.2:c.346+4_346+5insT	NP_001229453.1:n.346+4_346+5insT
NM_001242525.2:c.346+4_346+5insT	NP_001229454.1:n.346+4_346+5insT