Canonical Allele Identifier: CA401363732

Gene: GAA

Linked Data

• ClinVar Variation Id: 495669
• ClinVar RCV Id: RCV000586360
• dbSNP Id: rs1555599713
• MyVariant Identifiers: chr17:g.78081523T>A (hg19) ; chr17:g.80107724T>A (hg38)
• PubMed: PMID:22252923

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80107724T>A , CM000679.2:g.80107724T>A	GRCh38
NC_000017.10:g.78081523T>A , CM000679.1:g.78081523T>A	GRCh37
NC_000017.9:g.75696118T>A	NCBI36
NG_009822.1:g.11169T>A , LRG_673:g.11169T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.858+2T>A	ENSP00000460543.2:n.858+2T>A
ENST00000572080.2:c.858+2T>A	ENSP00000459972.2:n.858+2T>A
ENST00000577106.6:c.858+2T>A	ENSP00000458306.2:n.858+2T>A
ENST00000302262.8:c.858+2T>A MANE Select	ENSP00000305692.3:n.858+2T>A
ENST00000302262.7:c.858+2T>A	ENSP00000305692.3:n.858+2T>A
ENST00000390015.7:c.858+2T>A	ENSP00000374665.3:n.858+2T>A
NM_000152.3:c.858+2T>A , LRG_673t1:c.858+2T>A	NP_000143.2:n.858+2T>A
NM_001079803.1:c.858+2T>A	NP_001073271.1:n.858+2T>A
NM_001079804.1:c.858+2T>A	NP_001073272.1:n.858+2T>A
XM_005257193.1:c.858+2T>A	XP_005257250.1:n.858+2T>A
XM_005257194.3:c.858+2T>A	XP_005257251.1:n.858+2T>A
NM_000152.4:c.858+2T>A	NP_000143.2:n.858+2T>A
NM_001079803.2:c.858+2T>A	NP_001073271.1:n.858+2T>A
NM_001079804.2:c.858+2T>A	NP_001073272.1:n.858+2T>A
XM_005257193.2:c.858+2T>A	XP_005257250.1:n.858+2T>A
XM_005257194.4:c.858+2T>A	XP_005257251.1:n.858+2T>A
NM_000152.5:c.858+2T>A MANE Select	NP_000143.2:n.858+2T>A
NM_001079803.3:c.858+2T>A	NP_001073271.1:n.858+2T>A
NM_001079804.3:c.858+2T>A	NP_001073272.1:n.858+2T>A