Canonical Allele Identifier: CA775505949

Gene: GAA

Linked Data

• dbSNP Id: rs1412888880
• gnomAD v3: 17-80101658-A-G
• gnomAD v4: 17-80101658-A-G
• MyVariant Identifiers: chr17:g.78075457A>G (hg19) ; chr17:g.80101658A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80101658A>G , CM000679.2:g.80101658A>G	GRCh38
NC_000017.10:g.78075457A>G , CM000679.1:g.78075457A>G	GRCh37
NC_000017.9:g.75690052A>G	NCBI36
NG_009822.1:g.5103A>G , LRG_673:g.5103A>G
NG_029761.1:g.70027A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000570803.6:c.-33+33A>G	ENSP00000460543.2:n.-33+33A>G
ENST00000572080.2:c.-113+33A>G	ENSP00000459972.2:n.-113+33A>G
ENST00000577106.6:c.-148+33A>G	ENSP00000458306.2:n.-148+33A>G
ENST00000302262.8:c.-265A>G MANE Select	ENSP00000305692.3:n.-265A>G
ENST00000390015.7:c.-113+33A>G	ENSP00000374665.3:n.-113+33A>G
ENST00000570803.5:c.-33+33A>G	ENSP00000460543.1:n.-33+33A>G
ENST00000574376.1:n.29+33A>G
ENST00000577106.5:c.-148+33A>G	ENSP00000458306.1:n.-148+33A>G
NM_000152.3:c.-265A>G , LRG_673t1:c.-265A>G	NP_000143.2:n.-265A>G
NM_001079803.1:c.-113+33A>G	NP_001073271.1:n.-113+33A>G
NM_001079804.1:c.-33+33A>G	NP_001073272.1:n.-33+33A>G
XM_005257193.1:c.-175A>G	XP_005257250.1:n.-175A>G
XM_005257194.3:c.-148+33A>G	XP_005257251.1:n.-148+33A>G
NM_000152.4:c.-265A>G	NP_000143.2:n.-265A>G
NM_001079803.2:c.-113+33A>G	NP_001073271.1:n.-113+33A>G
NM_001079804.2:c.-33+33A>G	NP_001073272.1:n.-33+33A>G
NR_134848.1:n.100+33A>G
XM_005257193.2:c.-175A>G	XP_005257250.1:n.-175A>G
XM_005257194.4:c.-148+33A>G	XP_005257251.1:n.-148+33A>G
NM_000152.5:c.-265A>G MANE Select	NP_000143.2:n.-265A>G
NM_001079803.3:c.-113+33A>G	NP_001073271.1:n.-113+33A>G
NM_001079804.3:c.-33+33A>G	NP_001073272.1:n.-33+33A>G
NR_134848.2:n.45+33A>G