Canonical Allele Identifier: CA273972

Gene: GAA

Linked Data

• ClinVar Variation Id: 188797
• ClinVar RCV Id: RCV000169127 ; RCV000723463
• dbSNP Id: rs543300039
• ExAC: 17:78081665 G / A
• gnomAD v2: 17-78081665-G-A
• gnomAD v3: 17-80107866-G-A
• gnomAD v4: 17-80107866-G-A
• MyVariant Identifiers: chr17:g.78081665G>A (hg19) ; chr17:g.80107866G>A (hg38)
• ERepo: CA273972/MONDO:0009290/010
• PubMed: PMID:9660056 ; PMID:16917947 ; PMID:17616415 ; PMID:23402890 ; PMID:23601496 ; PMID:23891399

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80107866G>A , CM000679.2:g.80107866G>A	GRCh38
NC_000017.10:g.78081665G>A , CM000679.1:g.78081665G>A	GRCh37
NC_000017.9:g.75696260G>A	NCBI36
NG_009822.1:g.11311G>A , LRG_673:g.11311G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.925G>A	ENSP00000460543.2:p.Gly309Arg
ENST00000572080.2:c.925G>A	ENSP00000459972.2:p.Gly309Arg
ENST00000577106.6:c.925G>A	ENSP00000458306.2:p.Gly309Arg
ENST00000302262.8:c.925G>A MANE Select	ENSP00000305692.3:p.Gly309Arg
ENST00000302262.7:c.925G>A	ENSP00000305692.3:p.Gly309Arg
ENST00000390015.7:c.925G>A	ENSP00000374665.3:p.Gly309Arg
NM_000152.3:c.925G>A , LRG_673t1:c.925G>A	NP_000143.2:p.Gly309Arg
NM_001079803.1:c.925G>A	NP_001073271.1:p.Gly309Arg
NM_001079804.1:c.925G>A	NP_001073272.1:p.Gly309Arg
XM_005257193.1:c.925G>A	XP_005257250.1:p.Gly309Arg
XM_005257194.3:c.925G>A	XP_005257251.1:p.Gly309Arg
NM_000152.4:c.925G>A	NP_000143.2:p.Gly309Arg
NM_001079803.2:c.925G>A	NP_001073271.1:p.Gly309Arg
NM_001079804.2:c.925G>A	NP_001073272.1:p.Gly309Arg
XM_005257193.2:c.925G>A	XP_005257250.1:p.Gly309Arg
XM_005257194.4:c.925G>A	XP_005257251.1:p.Gly309Arg
NM_000152.5:c.925G>A MANE Select	NP_000143.2:p.Gly309Arg
NM_001079803.3:c.925G>A	NP_001073271.1:p.Gly309Arg
NM_001079804.3:c.925G>A	NP_001073272.1:p.Gly309Arg