Canonical Allele Identifier: CA137040671

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs143038309
• gnomAD v2: 6-33037833-A-T
• gnomAD v3: 6-33070056-A-T
• gnomAD v4: 6-33070056-A-T
• MyVariant Identifiers: chr6:g.33037833A>T (hg19) ; chr6:g.33070056A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33070056A>T , CM000668.2:g.33070056A>T	GRCh38
NC_000006.11:g.33037833A>T , CM000668.1:g.33037833A>T	GRCh37
NC_000006.10:g.33145811A>T	NCBI36
NG_033241.1:g.15723T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692443.1:c.101-170T>A MANE Select	ENSP00000509163.1:n.101-170T>A
ENST00000419277.5:c.101-170T>A	ENSP00000393566.1:n.101-170T>A
ENST00000453337.1:c.101-170T>A	ENSP00000390929.1:n.101-170T>A
ENST00000463066.1:n.196-170T>A
ENST00000476642.5:n.77-170T>A
ENST00000479107.1:n.146-170T>A
NM_001242524.1:c.101-170T>A	NP_001229453.1:n.101-170T>A
NM_001242525.1:c.101-170T>A	NP_001229454.1:n.101-170T>A
NM_033554.3:c.101-170T>A	NP_291032.2:n.101-170T>A
XM_011514559.1:c.101-170T>A	XP_011512861.1:n.101-170T>A
NM_001242524.2:c.101-170T>A	NP_001229453.1:n.101-170T>A
NM_001242525.2:c.101-170T>A	NP_001229454.1:n.101-170T>A