Canonical Allele Identifier: CA2640269517

Gene: GAA

Linked Data

• gnomAD v4: 17-80101597-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80101597G>T , CM000679.2:g.80101597G>T	GRCh38
NC_000017.10:g.78075396G>T , CM000679.1:g.78075396G>T	GRCh37
NC_000017.9:g.75689991G>T	NCBI36
NG_009822.1:g.5042G>T , LRG_673:g.5042G>T
NG_029761.1:g.69966G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.-61G>T	ENSP00000460543.2:n.-61G>T
ENST00000572080.2:c.-141G>T	ENSP00000459972.2:n.-141G>T
ENST00000577106.6:c.-176G>T	ENSP00000458306.2:n.-176G>T
ENST00000302262.8:c.-326G>T MANE Select	ENSP00000305692.3:n.-326G>T
ENST00000390015.7:c.-141G>T	ENSP00000374665.3:n.-141G>T
ENST00000570803.5:c.-61G>T	ENSP00000460543.1:n.-61G>T
ENST00000574376.1:n.1G>T
ENST00000577106.5:c.-176G>T	ENSP00000458306.1:n.-176G>T
NM_000152.3:c.-326G>T , LRG_673t1:c.-326G>T	NP_000143.2:n.-326G>T
NM_001079803.1:c.-141G>T	NP_001073271.1:n.-141G>T
NM_001079804.1:c.-61G>T	NP_001073272.1:n.-61G>T
XM_005257194.3:c.-176G>T	XP_005257251.1:n.-176G>T
NM_000152.4:c.-326G>T	NP_000143.2:n.-326G>T
NM_001079803.2:c.-141G>T	NP_001073271.1:n.-141G>T
NM_001079804.2:c.-61G>T	NP_001073272.1:n.-61G>T
NR_134848.1:n.72G>T
XM_005257194.4:c.-176G>T	XP_005257251.1:n.-176G>T
NM_000152.5:c.-326G>T MANE Select	NP_000143.2:n.-326G>T
NM_001079803.3:c.-141G>T	NP_001073271.1:n.-141G>T
NM_001079804.3:c.-61G>T	NP_001073272.1:n.-61G>T
NR_134848.2:n.17G>T