Canonical Allele Identifier: CA658795228
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2736671
ClinVar RCV Id: RCV003502024
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80105010_80105026del , CM000679.2:g.80105010_80105026del GRCh38
NC_000017.10:g.78078809_78078825del , CM000679.1:g.78078809_78078825del GRCh37
NC_000017.9:g.75693404_75693420del NCBI36
NG_009822.1:g.8455_8471del , LRG_673:g.8455_8471del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.424_440del ENSP00000460543.2:p.Ser142LeufsTer29
ENST00000572080.2:c.424_440del ENSP00000459972.2:p.Ser142LeufsTer29
ENST00000577106.6:c.424_440del ENSP00000458306.2:p.Ser142LeufsTer29
ENST00000302262.8:c.424_440del MANE Select ENSP00000305692.3:p.Ser142LeufsTer29
ENST00000302262.7:c.424_440del ENSP00000305692.3:p.Ser142LeufsTer29
ENST00000390015.7:c.424_440del ENSP00000374665.3:p.Ser142LeufsTer29
ENST00000570803.5:c.424_440del ENSP00000460543.1:p.Ser142LeufsTer29
ENST00000577106.5:c.424_440del ENSP00000458306.1:p.Ser142LeufsTer29
NM_000152.3:c.424_440del , LRG_673t1:c.424_440del NP_000143.2:p.Ser142LeufsTer29
NM_001079803.1:c.424_440del NP_001073271.1:p.Ser142LeufsTer29
NM_001079804.1:c.424_440del NP_001073272.1:p.Ser142LeufsTer29
XM_005257193.1:c.424_440del XP_005257250.1:p.Ser142LeufsTer29
XM_005257194.3:c.424_440del XP_005257251.1:p.Ser142LeufsTer29
NM_000152.4:c.424_440del NP_000143.2:p.Ser142LeufsTer29
NM_001079803.2:c.424_440del NP_001073271.1:p.Ser142LeufsTer29
NM_001079804.2:c.424_440del NP_001073272.1:p.Ser142LeufsTer29
XM_005257193.2:c.424_440del XP_005257250.1:p.Ser142LeufsTer29
XM_005257194.4:c.424_440del XP_005257251.1:p.Ser142LeufsTer29
NM_000152.5:c.424_440del MANE Select NP_000143.2:p.Ser142LeufsTer29
NM_001079803.3:c.424_440del NP_001073271.1:p.Ser142LeufsTer29
NM_001079804.3:c.424_440del NP_001073272.1:p.Ser142LeufsTer29
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