Canonical Allele Identifier: CA891844474

Gene: GAA

Linked Data

• ClinVar Variation Id: 578596
• ClinVar RCV Id: RCV000701657
• dbSNP Id: rs1567833173
• MyVariant Identifiers: chr17:g.78084726_78084739del (hg19) ; chr17:g.80110927_80110940del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80110927_80110940del , CM000679.2:g.80110927_80110940del	GRCh38
NC_000017.10:g.78084726_78084739del , CM000679.1:g.78084726_78084739del	GRCh37
NC_000017.9:g.75699321_75699334del	NCBI36
NG_009822.1:g.14372_14385del , LRG_673:g.14372_14385del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.1552-14_1552-1del	ENSP00000460543.2:n.1552-14_1552-1del
ENST00000572080.2:c.1552-14_1552-1del	ENSP00000459972.2:n.1552-14_1552-1del
ENST00000577106.6:c.1552-14_1552-1del	ENSP00000458306.2:n.1552-14_1552-1del
ENST00000302262.8:c.1552-14_1552-1del MANE Select	ENSP00000305692.3:n.1552-14_1552-1del
ENST00000302262.7:c.1552-14_1552-1del	ENSP00000305692.3:n.1552-14_1552-1del
ENST00000390015.7:c.1552-14_1552-1del	ENSP00000374665.3:n.1552-14_1552-1del
NM_000152.3:c.1552-14_1552-1del , LRG_673t1:c.1552-14_1552-1del	NP_000143.2:n.1552-14_1552-1del
NM_001079803.1:c.1552-14_1552-1del	NP_001073271.1:n.1552-14_1552-1del
NM_001079804.1:c.1552-14_1552-1del	NP_001073272.1:n.1552-14_1552-1del
XM_005257193.1:c.1552-14_1552-1del	XP_005257250.1:n.1552-14_1552-1del
XM_005257194.3:c.1552-14_1552-1del	XP_005257251.1:n.1552-14_1552-1del
NM_000152.4:c.1552-14_1552-1del	NP_000143.2:n.1552-14_1552-1del
NM_001079803.2:c.1552-14_1552-1del	NP_001073271.1:n.1552-14_1552-1del
NM_001079804.2:c.1552-14_1552-1del	NP_001073272.1:n.1552-14_1552-1del
XM_005257193.2:c.1552-14_1552-1del	XP_005257250.1:n.1552-14_1552-1del
XM_005257194.4:c.1552-14_1552-1del	XP_005257251.1:n.1552-14_1552-1del
NM_000152.5:c.1552-14_1552-1del MANE Select	NP_000143.2:n.1552-14_1552-1del
NM_001079803.3:c.1552-14_1552-1del	NP_001073271.1:n.1552-14_1552-1del
NM_001079804.3:c.1552-14_1552-1del	NP_001073272.1:n.1552-14_1552-1del