Canonical Allele Identifier: CA10647066

Gene: GAA

Linked Data

• ClinVar Variation Id: 325797
• ClinVar RCV Id: RCV000269141
• dbSNP Id: rs886053547
• MyVariant Identifiers: chr17:g.78093062C>G (hg19) ; chr17:g.80119263C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80119263C>G , CM000679.2:g.80119263C>G	GRCh38
NC_000017.10:g.78093062C>G , CM000679.1:g.78093062C>G	GRCh37
NC_000017.9:g.75707657C>G	NCBI36
NG_009822.1:g.22708C>G , LRG_673:g.22708C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.2800-9C>G	ENSP00000460543.2:n.2800-9C>G
ENST00000572080.2:c.*938-9C>G	ENSP00000459972.2:n.*938-9C>G
ENST00000577106.6:c.2800-9C>G	ENSP00000458306.2:n.2800-9C>G
ENST00000302262.8:c.2800-9C>G MANE Select	ENSP00000305692.3:n.2800-9C>G
ENST00000302262.7:c.2800-9C>G	ENSP00000305692.3:n.2800-9C>G
ENST00000390015.7:c.2800-9C>G	ENSP00000374665.3:n.2800-9C>G
ENST00000573556.1:n.753-9C>G
NM_000152.3:c.2800-9C>G , LRG_673t1:c.2800-9C>G	NP_000143.2:n.2800-9C>G
NM_001079803.1:c.2800-9C>G	NP_001073271.1:n.2800-9C>G
NM_001079804.1:c.2800-9C>G	NP_001073272.1:n.2800-9C>G
XM_005257193.1:c.2800-9C>G	XP_005257250.1:n.2800-9C>G
XM_005257194.3:c.2800-9C>G	XP_005257251.1:n.2800-9C>G
NM_000152.4:c.2800-9C>G	NP_000143.2:n.2800-9C>G
NM_001079803.2:c.2800-9C>G	NP_001073271.1:n.2800-9C>G
NM_001079804.2:c.2800-9C>G	NP_001073272.1:n.2800-9C>G
XM_005257193.2:c.2800-9C>G	XP_005257250.1:n.2800-9C>G
XM_005257194.4:c.2800-9C>G	XP_005257251.1:n.2800-9C>G
NM_000152.5:c.2800-9C>G MANE Select	NP_000143.2:n.2800-9C>G
NM_001079803.3:c.2800-9C>G	NP_001073271.1:n.2800-9C>G
NM_001079804.3:c.2800-9C>G	NP_001073272.1:n.2800-9C>G