Canonical Allele Identifier: CA8814957

Gene: GAA

Linked Data

• ClinVar Variation Id: 290223
• ClinVar RCV Id: RCV000287222 ; RCV000631099 ; RCV001705433
• dbSNP Id: rs374569672
• ExAC: 17:78079665 G / A
• gnomAD v2: 17-78079665-G-A
• gnomAD v3: 17-80105866-G-A
• gnomAD v4: 17-80105866-G-A
• MyVariant Identifiers: chr17:g.78079665G>A (hg19) ; chr17:g.80105866G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80105866G>A , CM000679.2:g.80105866G>A	GRCh38
NC_000017.10:g.78079665G>A , CM000679.1:g.78079665G>A	GRCh37
NC_000017.9:g.75694260G>A	NCBI36
NG_009822.1:g.9311G>A , LRG_673:g.9311G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000570803.6:c.664G>A	ENSP00000460543.2:p.Val222Met
ENST00000572080.2:c.664G>A	ENSP00000459972.2:p.Val222Met
ENST00000577106.6:c.664G>A	ENSP00000458306.2:p.Val222Met
ENST00000302262.8:c.664G>A MANE Select	ENSP00000305692.3:p.Val222Met
ENST00000302262.7:c.664G>A	ENSP00000305692.3:p.Val222Met
ENST00000390015.7:c.664G>A	ENSP00000374665.3:p.Val222Met
ENST00000570803.5:c.664G>A	ENSP00000460543.1:p.Val222Met
NM_000152.3:c.664G>A , LRG_673t1:c.664G>A	NP_000143.2:p.Val222Met
NM_001079803.1:c.664G>A	NP_001073271.1:p.Val222Met
NM_001079804.1:c.664G>A	NP_001073272.1:p.Val222Met
XM_005257193.1:c.664G>A	XP_005257250.1:p.Val222Met
XM_005257194.3:c.664G>A	XP_005257251.1:p.Val222Met
NM_000152.4:c.664G>A	NP_000143.2:p.Val222Met
NM_001079803.2:c.664G>A	NP_001073271.1:p.Val222Met
NM_001079804.2:c.664G>A	NP_001073272.1:p.Val222Met
XM_005257193.2:c.664G>A	XP_005257250.1:p.Val222Met
XM_005257194.4:c.664G>A	XP_005257251.1:p.Val222Met
NM_000152.5:c.664G>A MANE Select	NP_000143.2:p.Val222Met
NM_001079803.3:c.664G>A	NP_001073271.1:p.Val222Met
NM_001079804.3:c.664G>A	NP_001073272.1:p.Val222Met