Canonical Allele Identifier: CA2695200359

Gene: GAA

Linked Data

• ClinVar Variation Id: 2675771
• ClinVar RCV Id: RCV003468232

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80118661_80118662delinsT , CM000679.2:g.80118661_80118662delinsT	GRCh38
NC_000017.10:g.78092460_78092461delinsT , CM000679.1:g.78092460_78092461delinsT	GRCh37
NC_000017.9:g.75707055_75707056delinsT	NCBI36
NG_009822.1:g.22106_22107delinsT , LRG_673:g.22106_22107delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.2655_2656delinsT	ENSP00000460543.2:p.Val886Ter
ENST00000572080.2:c.*793_*794delinsT	ENSP00000459972.2:n.*793_*794delinsT
ENST00000577106.6:c.2655_2656delinsT	ENSP00000458306.2:p.Val886Ter
ENST00000302262.8:c.2655_2656delinsT MANE Select	ENSP00000305692.3:p.Val886Ter
ENST00000302262.7:c.2655_2656delinsT	ENSP00000305692.3:p.Val886Ter
ENST00000390015.7:c.2655_2656delinsT	ENSP00000374665.3:p.Val886Ter
ENST00000573556.1:n.608_609delinsT
NM_000152.3:c.2655_2656delinsT , LRG_673t1:c.2655_2656delinsT	NP_000143.2:p.Val886Ter
NM_001079803.1:c.2655_2656delinsT	NP_001073271.1:p.Val886Ter
NM_001079804.1:c.2655_2656delinsT	NP_001073272.1:p.Val886Ter
XM_005257193.1:c.2655_2656delinsT	XP_005257250.1:p.Val886Ter
XM_005257194.3:c.2655_2656delinsT	XP_005257251.1:p.Val886Ter
NM_000152.4:c.2655_2656delinsT	NP_000143.2:p.Val886Ter
NM_001079803.2:c.2655_2656delinsT	NP_001073271.1:p.Val886Ter
NM_001079804.2:c.2655_2656delinsT	NP_001073272.1:p.Val886Ter
XM_005257193.2:c.2655_2656delinsT	XP_005257250.1:p.Val886Ter
XM_005257194.4:c.2655_2656delinsT	XP_005257251.1:p.Val886Ter
NM_000152.5:c.2655_2656delinsT MANE Select	NP_000143.2:p.Val886Ter
NM_001079803.3:c.2655_2656delinsT	NP_001073271.1:p.Val886Ter
NM_001079804.3:c.2655_2656delinsT	NP_001073272.1:p.Val886Ter