Canonical Allele Identifier: CA502168776

Gene: GAA

Linked Data

• ClinVar Variation Id: 1626821
• ClinVar RCV Id: RCV002120607
• dbSNP Id: rs2039415234
• gnomAD v4: 17-80118712-G-A
• MyVariant Identifiers: chr17:g.78092511G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80118712G>A , CM000679.2:g.80118712G>A	GRCh38
NC_000017.10:g.78092511G>A , CM000679.1:g.78092511G>A	GRCh37
NC_000017.9:g.75707106G>A	NCBI36
NG_009822.1:g.22157G>A , LRG_673:g.22157G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000570803.6:c.2706G>A	ENSP00000460543.2:p.Gln902=
ENST00000572080.2:c.*844G>A	ENSP00000459972.2:n.*844G>A
ENST00000577106.6:c.2706G>A	ENSP00000458306.2:p.Gln902=
ENST00000302262.8:c.2706G>A MANE Select	ENSP00000305692.3:p.Gln902=
ENST00000302262.7:c.2706G>A	ENSP00000305692.3:p.Gln902=
ENST00000390015.7:c.2706G>A	ENSP00000374665.3:p.Gln902=
ENST00000573556.1:n.659G>A
NM_000152.3:c.2706G>A , LRG_673t1:c.2706G>A	NP_000143.2:p.Gln902=
NM_001079803.1:c.2706G>A	NP_001073271.1:p.Gln902=
NM_001079804.1:c.2706G>A	NP_001073272.1:p.Gln902=
XM_005257193.1:c.2706G>A	XP_005257250.1:p.Gln902=
XM_005257194.3:c.2706G>A	XP_005257251.1:p.Gln902=
NM_000152.4:c.2706G>A	NP_000143.2:p.Gln902=
NM_001079803.2:c.2706G>A	NP_001073271.1:p.Gln902=
NM_001079804.2:c.2706G>A	NP_001073272.1:p.Gln902=
XM_005257193.2:c.2706G>A	XP_005257250.1:p.Gln902=
XM_005257194.4:c.2706G>A	XP_005257251.1:p.Gln902=
NM_000152.5:c.2706G>A MANE Select	NP_000143.2:p.Gln902=
NM_001079803.3:c.2706G>A	NP_001073271.1:p.Gln902=
NM_001079804.3:c.2706G>A	NP_001073272.1:p.Gln902=