Canonical Allele Identifier: CA401363637

Gene: GAA

Linked Data

• ClinVar Variation Id: 928706
• ClinVar RCV Id: RCV001193013
• dbSNP Id: rs2039122730
• MyVariant Identifiers: chr17:g.78081499G>A (hg19) ; chr17:g.80107700G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80107700G>A , CM000679.2:g.80107700G>A	GRCh38
NC_000017.10:g.78081499G>A , CM000679.1:g.78081499G>A	GRCh37
NC_000017.9:g.75696094G>A	NCBI36
NG_009822.1:g.11145G>A , LRG_673:g.11145G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.836G>A	ENSP00000460543.2:p.Trp279Ter
ENST00000572080.2:c.836G>A	ENSP00000459972.2:p.Trp279Ter
ENST00000577106.6:c.836G>A	ENSP00000458306.2:p.Trp279Ter
ENST00000302262.8:c.836G>A MANE Select	ENSP00000305692.3:p.Trp279Ter
ENST00000302262.7:c.836G>A	ENSP00000305692.3:p.Trp279Ter
ENST00000390015.7:c.836G>A	ENSP00000374665.3:p.Trp279Ter
ENST00000570803.5:c.836G>A	ENSP00000460543.1:p.Trp279Ter
NM_000152.3:c.836G>A , LRG_673t1:c.836G>A	NP_000143.2:p.Trp279Ter
NM_001079803.1:c.836G>A	NP_001073271.1:p.Trp279Ter
NM_001079804.1:c.836G>A	NP_001073272.1:p.Trp279Ter
XM_005257193.1:c.836G>A	XP_005257250.1:p.Trp279Ter
XM_005257194.3:c.836G>A	XP_005257251.1:p.Trp279Ter
NM_000152.4:c.836G>A	NP_000143.2:p.Trp279Ter
NM_001079803.2:c.836G>A	NP_001073271.1:p.Trp279Ter
NM_001079804.2:c.836G>A	NP_001073272.1:p.Trp279Ter
XM_005257193.2:c.836G>A	XP_005257250.1:p.Trp279Ter
XM_005257194.4:c.836G>A	XP_005257251.1:p.Trp279Ter
NM_000152.5:c.836G>A MANE Select	NP_000143.2:p.Trp279Ter
NM_001079803.3:c.836G>A	NP_001073271.1:p.Trp279Ter
NM_001079804.3:c.836G>A	NP_001073272.1:p.Trp279Ter