Canonical Allele Identifier: CA658824775
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 554096
dbSNP Id: rs1555598869
MyVariant Identifiers: chr17:g.80105023del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80105023del , CM000679.2:g.80105023del GRCh38
NC_000017.10:g.78078822del , CM000679.1:g.78078822del GRCh37
NC_000017.9:g.75693417del NCBI36
NG_009822.1:g.8468del , LRG_673:g.8468del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.437del ENSP00000460543.2:p.Met146ArgfsTer7
ENST00000572080.2:c.437del ENSP00000459972.2:p.Met146ArgfsTer7
ENST00000577106.6:c.437del ENSP00000458306.2:p.Met146ArgfsTer7
ENST00000302262.8:c.437del MANE Select ENSP00000305692.3:p.Met146ArgfsTer7
ENST00000302262.7:c.437del ENSP00000305692.3:p.Met146ArgfsTer7
ENST00000390015.7:c.437del ENSP00000374665.3:p.Met146ArgfsTer7
ENST00000570803.5:c.437del ENSP00000460543.1:p.Met146ArgfsTer7
ENST00000577106.5:c.437del ENSP00000458306.1:p.Met146ArgfsTer7
NM_000152.3:c.437del , LRG_673t1:c.437del NP_000143.2:p.Met146ArgfsTer7
NM_001079803.1:c.437del NP_001073271.1:p.Met146ArgfsTer7
NM_001079804.1:c.437del NP_001073272.1:p.Met146ArgfsTer7
XM_005257193.1:c.437del XP_005257250.1:p.Met146ArgfsTer7
XM_005257194.3:c.437del XP_005257251.1:p.Met146ArgfsTer7
NM_000152.4:c.437del NP_000143.2:p.Met146ArgfsTer7
NM_001079803.2:c.437del NP_001073271.1:p.Met146ArgfsTer7
NM_001079804.2:c.437del NP_001073272.1:p.Met146ArgfsTer7
XM_005257193.2:c.437del XP_005257250.1:p.Met146ArgfsTer7
XM_005257194.4:c.437del XP_005257251.1:p.Met146ArgfsTer7
NM_000152.5:c.437del MANE Select NP_000143.2:p.Met146ArgfsTer7
NM_001079803.3:c.437del NP_001073271.1:p.Met146ArgfsTer7
NM_001079804.3:c.437del NP_001073272.1:p.Met146ArgfsTer7