Canonical Allele Identifier: CA502167637

Gene: GAA

Linked Data

• ClinVar Variation Id: 1142659
• ClinVar RCV Id: RCV001480556
• dbSNP Id: rs780321415
• gnomAD v3: 17-80118319-C-A
• gnomAD v4: 17-80118319-C-A
• MyVariant Identifiers: chr17:g.78092118C>A (hg19) ; chr17:g.80118319C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80118319C>A , CM000679.2:g.80118319C>A	GRCh38
NC_000017.10:g.78092118C>A , CM000679.1:g.78092118C>A	GRCh37
NC_000017.9:g.75706713C>A	NCBI36
NG_009822.1:g.21764C>A , LRG_673:g.21764C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000570803.6:c.2608C>A	ENSP00000460543.2:p.Arg870=
ENST00000572080.2:c.*746C>A	ENSP00000459972.2:n.*746C>A
ENST00000577106.6:c.2608C>A	ENSP00000458306.2:p.Arg870=
ENST00000302262.8:c.2608C>A MANE Select	ENSP00000305692.3:p.Arg870=
ENST00000302262.7:c.2608C>A	ENSP00000305692.3:p.Arg870=
ENST00000390015.7:c.2608C>A	ENSP00000374665.3:p.Arg870=
ENST00000573556.1:n.561C>A
NM_000152.3:c.2608C>A , LRG_673t1:c.2608C>A	NP_000143.2:p.Arg870=
NM_001079803.1:c.2608C>A	NP_001073271.1:p.Arg870=
NM_001079804.1:c.2608C>A	NP_001073272.1:p.Arg870=
XM_005257193.1:c.2608C>A	XP_005257250.1:p.Arg870=
XM_005257194.3:c.2608C>A	XP_005257251.1:p.Arg870=
NM_000152.4:c.2608C>A	NP_000143.2:p.Arg870=
NM_001079803.2:c.2608C>A	NP_001073271.1:p.Arg870=
NM_001079804.2:c.2608C>A	NP_001073272.1:p.Arg870=
XM_005257193.2:c.2608C>A	XP_005257250.1:p.Arg870=
XM_005257194.4:c.2608C>A	XP_005257251.1:p.Arg870=
NM_000152.5:c.2608C>A MANE Select	NP_000143.2:p.Arg870=
NM_001079803.3:c.2608C>A	NP_001073271.1:p.Arg870=
NM_001079804.3:c.2608C>A	NP_001073272.1:p.Arg870=