Canonical Allele Identifier: CA401364945

Gene: GAA

Linked Data

• ClinVar Variation Id: 1359350
• ClinVar RCV Id: RCV001904391
• dbSNP Id: rs2143854757
• MyVariant Identifiers: chr17:g.78082309A>C (hg19) ; chr17:g.80108510A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80108510A>C , CM000679.2:g.80108510A>C	GRCh38
NC_000017.10:g.78082309A>C , CM000679.1:g.78082309A>C	GRCh37
NC_000017.9:g.75696904A>C	NCBI36
NG_009822.1:g.11955A>C , LRG_673:g.11955A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000570803.6:c.1097A>C	ENSP00000460543.2:p.Tyr366Ser
ENST00000572080.2:c.1097A>C	ENSP00000459972.2:p.Tyr366Ser
ENST00000577106.6:c.1097A>C	ENSP00000458306.2:p.Tyr366Ser
ENST00000302262.8:c.1097A>C MANE Select	ENSP00000305692.3:p.Tyr366Ser
ENST00000302262.7:c.1097A>C	ENSP00000305692.3:p.Tyr366Ser
ENST00000390015.7:c.1097A>C	ENSP00000374665.3:p.Tyr366Ser
NM_000152.3:c.1097A>C , LRG_673t1:c.1097A>C	NP_000143.2:p.Tyr366Ser
NM_001079803.1:c.1097A>C	NP_001073271.1:p.Tyr366Ser
NM_001079804.1:c.1097A>C	NP_001073272.1:p.Tyr366Ser
XM_005257193.1:c.1097A>C	XP_005257250.1:p.Tyr366Ser
XM_005257194.3:c.1097A>C	XP_005257251.1:p.Tyr366Ser
NM_000152.4:c.1097A>C	NP_000143.2:p.Tyr366Ser
NM_001079803.2:c.1097A>C	NP_001073271.1:p.Tyr366Ser
NM_001079804.2:c.1097A>C	NP_001073272.1:p.Tyr366Ser
XM_005257193.2:c.1097A>C	XP_005257250.1:p.Tyr366Ser
XM_005257194.4:c.1097A>C	XP_005257251.1:p.Tyr366Ser
NM_000152.5:c.1097A>C MANE Select	NP_000143.2:p.Tyr366Ser
NM_001079803.3:c.1097A>C	NP_001073271.1:p.Tyr366Ser
NM_001079804.3:c.1097A>C	NP_001073272.1:p.Tyr366Ser