Canonical Allele Identifier: CA658795291
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 657307
dbSNP Id: rs1598592604

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80117859_80118396del , CM000679.2:g.80117859_80118396del GRCh38
NC_000017.10:g.78091658_78092195del , CM000679.1:g.78091658_78092195del GRCh37
NC_000017.9:g.75706253_75706790del NCBI36
NG_009822.1:g.21304_21841del , LRG_673:g.21304_21841del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2481+110_2646+39del
ENST00000572080.2:c.*619+110_*784+39del
ENST00000577106.6:c.2481+110_2646+39del
ENST00000302262.8:c.2481+110_2646+39del
ENST00000302262.7:c.2481+110_2646+39del
ENST00000390015.7:c.2481+110_2646+39del
ENST00000573556.1:n.434+110_599+39del
NM_000152.3:c.2481+110_2646+39del , LRG_673t1:c.2481+110_2646+39del
NM_001079803.1:c.2481+110_2646+39del
NM_001079804.1:c.2481+110_2646+39del
XM_005257193.1:c.2481+110_2646+39del
XM_005257194.3:c.2481+110_2646+39del
NM_000152.4:c.2481+110_2646+39del
NM_001079803.2:c.2481+110_2646+39del
NM_001079804.2:c.2481+110_2646+39del
XM_005257193.2:c.2481+110_2646+39del
XM_005257194.4:c.2481+110_2646+39del
NM_000152.5:c.2481+110_2646+39del
NM_001079803.3:c.2481+110_2646+39del
NM_001079804.3:c.2481+110_2646+39del