Canonical Allele Identifier: CA2277808991

Gene: GAA

Linked Data

• dbSNP Id: rs2038948793
• gnomAD v4: 17-80101588-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80101588G>A , CM000679.2:g.80101588G>A	GRCh38
NC_000017.10:g.78075387G>A , CM000679.1:g.78075387G>A	GRCh37
NC_000017.9:g.75689982G>A	NCBI36
NG_009822.1:g.5033G>A , LRG_673:g.5033G>A
NG_029761.1:g.69957G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.-70G>A	ENSP00000460543.2:n.-70G>A
ENST00000572080.2:c.-150G>A	ENSP00000459972.2:n.-150G>A
ENST00000577106.6:c.-185G>A	ENSP00000458306.2:n.-185G>A
ENST00000302262.8:c.-335G>A MANE Select	ENSP00000305692.3:n.-335G>A
ENST00000570803.5:c.-70G>A	ENSP00000460543.1:n.-70G>A
ENST00000577106.5:c.-185G>A	ENSP00000458306.1:n.-185G>A
NM_000152.3:c.-335G>A , LRG_673t1:c.-335G>A	NP_000143.2:n.-335G>A
NM_001079803.1:c.-150G>A	NP_001073271.1:n.-150G>A
NM_001079804.1:c.-70G>A	NP_001073272.1:n.-70G>A
XM_005257194.3:c.-185G>A	XP_005257251.1:n.-185G>A
NM_000152.4:c.-335G>A	NP_000143.2:n.-335G>A
NM_001079803.2:c.-150G>A	NP_001073271.1:n.-150G>A
NM_001079804.2:c.-70G>A	NP_001073272.1:n.-70G>A
NR_134848.1:n.63G>A
XM_005257194.4:c.-185G>A	XP_005257251.1:n.-185G>A
NM_000152.5:c.-335G>A MANE Select	NP_000143.2:n.-335G>A
NM_001079803.3:c.-150G>A	NP_001073271.1:n.-150G>A
NM_001079804.3:c.-70G>A	NP_001073272.1:n.-70G>A
NR_134848.2:n.8G>A