Canonical Allele Identifier: CA2640269548

Gene: GAA

Linked Data

• gnomAD v4: 17-80101607-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80101607A>G , CM000679.2:g.80101607A>G	GRCh38
NC_000017.10:g.78075406A>G , CM000679.1:g.78075406A>G	GRCh37
NC_000017.9:g.75690001A>G	NCBI36
NG_009822.1:g.5052A>G , LRG_673:g.5052A>G
NG_029761.1:g.69976A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.-51A>G	ENSP00000460543.2:n.-51A>G
ENST00000572080.2:c.-131A>G	ENSP00000459972.2:n.-131A>G
ENST00000577106.6:c.-166A>G	ENSP00000458306.2:n.-166A>G
ENST00000302262.8:c.-316A>G MANE Select	ENSP00000305692.3:n.-316A>G
ENST00000390015.7:c.-131A>G	ENSP00000374665.3:n.-131A>G
ENST00000570803.5:c.-51A>G	ENSP00000460543.1:n.-51A>G
ENST00000574376.1:n.11A>G
ENST00000577106.5:c.-166A>G	ENSP00000458306.1:n.-166A>G
NM_000152.3:c.-316A>G , LRG_673t1:c.-316A>G	NP_000143.2:n.-316A>G
NM_001079803.1:c.-131A>G	NP_001073271.1:n.-131A>G
NM_001079804.1:c.-51A>G	NP_001073272.1:n.-51A>G
XM_005257194.3:c.-166A>G	XP_005257251.1:n.-166A>G
NM_000152.4:c.-316A>G	NP_000143.2:n.-316A>G
NM_001079803.2:c.-131A>G	NP_001073271.1:n.-131A>G
NM_001079804.2:c.-51A>G	NP_001073272.1:n.-51A>G
NR_134848.1:n.82A>G
XM_005257194.4:c.-166A>G	XP_005257251.1:n.-166A>G
NM_000152.5:c.-316A>G MANE Select	NP_000143.2:n.-316A>G
NM_001079803.3:c.-131A>G	NP_001073271.1:n.-131A>G
NM_001079804.3:c.-51A>G	NP_001073272.1:n.-51A>G
NR_134848.2:n.27A>G