Canonical Allele Identifier: CA502167491
Gene: GAA HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.78092084del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80118285del , CM000679.2:g.80118285del GRCh38
NC_000017.10:g.78092084del , CM000679.1:g.78092084del GRCh37
NC_000017.9:g.75706679del NCBI36
NG_009822.1:g.21730del , LRG_673:g.21730del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2574del ENSP00000460543.2:p.Trp859GlyfsTer28
ENST00000572080.2:c.*712del ENSP00000459972.2:n.*712del
ENST00000577106.6:c.2574del ENSP00000458306.2:p.Trp859GlyfsTer28
ENST00000302262.8:c.2574del MANE Select ENSP00000305692.3:p.Trp859GlyfsTer28
ENST00000302262.7:c.2574del ENSP00000305692.3:p.Trp859GlyfsTer28
ENST00000390015.7:c.2574del ENSP00000374665.3:p.Trp859GlyfsTer28
ENST00000573556.1:n.527del
NM_000152.3:c.2574del , LRG_673t1:c.2574del NP_000143.2:p.Trp859GlyfsTer28
NM_001079803.1:c.2574del NP_001073271.1:p.Trp859GlyfsTer28
NM_001079804.1:c.2574del NP_001073272.1:p.Trp859GlyfsTer28
XM_005257193.1:c.2574del XP_005257250.1:p.Trp859GlyfsTer28
XM_005257194.3:c.2574del XP_005257251.1:p.Trp859GlyfsTer28
NM_000152.4:c.2574del NP_000143.2:p.Trp859GlyfsTer28
NM_001079803.2:c.2574del NP_001073271.1:p.Trp859GlyfsTer28
NM_001079804.2:c.2574del NP_001073272.1:p.Trp859GlyfsTer28
XM_005257193.2:c.2574del XP_005257250.1:p.Trp859GlyfsTer28
XM_005257194.4:c.2574del XP_005257251.1:p.Trp859GlyfsTer28
NM_000152.5:c.2574del MANE Select NP_000143.2:p.Trp859GlyfsTer28
NM_001079803.3:c.2574del NP_001073271.1:p.Trp859GlyfsTer28
NM_001079804.3:c.2574del NP_001073272.1:p.Trp859GlyfsTer28