Canonical Allele Identifier: CA2277810926

Gene: GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80105230_80105242delinsCTGTGTGCTGGGC , CM000679.2:g.80105230_80105242delinsCTGTGTGCTGGGC	GRCh38
NC_000017.10:g.78079029_78079041delinsCTGTGTGCTGGGC , CM000679.1:g.78079029_78079041delinsCTGTGTGCTGGGC	GRCh37
NC_000017.9:g.75693624_75693636delinsCTGTGTGCTGGGC	NCBI36
NG_009822.1:g.8675_8687delinsCTGTGTGCTGGGC , LRG_673:g.8675_8687delinsCTGTGTGCTGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.546+98_546+110delinsCTGTGTGCTGGGC	ENSP00000460543.2:n.546+98_546+110delinsCTGTGTGCTGGGC
ENST00000572080.2:c.546+98_546+110delinsCTGTGTGCTGGGC	ENSP00000459972.2:n.546+98_546+110delinsCTGTGTGCTGGGC
ENST00000577106.6:c.546+98_546+110delinsCTGTGTGCTGGGC	ENSP00000458306.2:n.546+98_546+110delinsCTGTGTGCTGGGC
ENST00000302262.8:c.546+98_546+110delinsCTGTGTGCTGGGC MANE Select	ENSP00000305692.3:n.546+98_546+110delinsCTGTGTGCTGGGC
ENST00000302262.7:c.546+98_546+110delinsCTGTGTGCTGGGC	ENSP00000305692.3:n.546+98_546+110delinsCTGTGTGCTGGGC
ENST00000390015.7:c.546+98_546+110delinsCTGTGTGCTGGGC	ENSP00000374665.3:n.546+98_546+110delinsCTGTGTGCTGGGC
ENST00000570803.5:c.546+98_546+110delinsCTGTGTGCTGGGC	ENSP00000460543.1:n.546+98_546+110delinsCTGTGTGCTGGGC
ENST00000577106.5:c.546+98_546+110delinsCTGTGTGCTGGGC	ENSP00000458306.1:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_000152.3:c.546+98_546+110delinsCTGTGTGCTGGGC , LRG_673t1:c.546+98_546+110delinsCTGTGTGCTGGGC	NP_000143.2:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_001079803.1:c.546+98_546+110delinsCTGTGTGCTGGGC	NP_001073271.1:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_001079804.1:c.546+98_546+110delinsCTGTGTGCTGGGC	NP_001073272.1:n.546+98_546+110delinsCTGTGTGCTGGGC
XM_005257193.1:c.546+98_546+110delinsCTGTGTGCTGGGC	XP_005257250.1:n.546+98_546+110delinsCTGTGTGCTGGGC
XM_005257194.3:c.546+98_546+110delinsCTGTGTGCTGGGC	XP_005257251.1:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_000152.4:c.546+98_546+110delinsCTGTGTGCTGGGC	NP_000143.2:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_001079803.2:c.546+98_546+110delinsCTGTGTGCTGGGC	NP_001073271.1:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_001079804.2:c.546+98_546+110delinsCTGTGTGCTGGGC	NP_001073272.1:n.546+98_546+110delinsCTGTGTGCTGGGC
XM_005257193.2:c.546+98_546+110delinsCTGTGTGCTGGGC	XP_005257250.1:n.546+98_546+110delinsCTGTGTGCTGGGC
XM_005257194.4:c.546+98_546+110delinsCTGTGTGCTGGGC	XP_005257251.1:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_000152.5:c.546+98_546+110delinsCTGTGTGCTGGGC MANE Select	NP_000143.2:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_001079803.3:c.546+98_546+110delinsCTGTGTGCTGGGC	NP_001073271.1:n.546+98_546+110delinsCTGTGTGCTGGGC
NM_001079804.3:c.546+98_546+110delinsCTGTGTGCTGGGC	NP_001073272.1:n.546+98_546+110delinsCTGTGTGCTGGGC