Canonical Allele Identifier: CA2580095780

Gene: GAA

Linked Data

• ClinVar Variation Id: 2098531
• ClinVar RCV Id: RCV003008480

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80112573C>T , CM000679.2:g.80112573C>T	GRCh38
NC_000017.10:g.78086372C>T , CM000679.1:g.78086372C>T	GRCh37
NC_000017.9:g.75700967C>T	NCBI36
NG_009822.1:g.16018C>T , LRG_673:g.16018C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000570803.6:c.1755-5C>T	ENSP00000460543.2:n.1755-5C>T
ENST00000572080.2:c.1755-5C>T	ENSP00000459972.2:n.1755-5C>T
ENST00000577106.6:c.1755-5C>T	ENSP00000458306.2:n.1755-5C>T
ENST00000302262.8:c.1755-5C>T MANE Select	ENSP00000305692.3:n.1755-5C>T
ENST00000302262.7:c.1755-5C>T	ENSP00000305692.3:n.1755-5C>T
ENST00000390015.7:c.1755-5C>T	ENSP00000374665.3:n.1755-5C>T
ENST00000570716.1:n.190C>T
ENST00000572080.1:c.143-5C>T
ENST00000572803.1:n.369-5C>T
NM_000152.3:c.1755-5C>T , LRG_673t1:c.1755-5C>T	NP_000143.2:n.1755-5C>T
NM_001079803.1:c.1755-5C>T	NP_001073271.1:n.1755-5C>T
NM_001079804.1:c.1755-5C>T	NP_001073272.1:n.1755-5C>T
XM_005257193.1:c.1755-5C>T	XP_005257250.1:n.1755-5C>T
XM_005257194.3:c.1755-5C>T	XP_005257251.1:n.1755-5C>T
NM_000152.4:c.1755-5C>T	NP_000143.2:n.1755-5C>T
NM_001079803.2:c.1755-5C>T	NP_001073271.1:n.1755-5C>T
NM_001079804.2:c.1755-5C>T	NP_001073272.1:n.1755-5C>T
XM_005257193.2:c.1755-5C>T	XP_005257250.1:n.1755-5C>T
XM_005257194.4:c.1755-5C>T	XP_005257251.1:n.1755-5C>T
NM_000152.5:c.1755-5C>T MANE Select	NP_000143.2:n.1755-5C>T
NM_001079803.3:c.1755-5C>T	NP_001073271.1:n.1755-5C>T
NM_001079804.3:c.1755-5C>T	NP_001073272.1:n.1755-5C>T