Canonical Allele Identifier: CA2277814334
Gene: GAA HGNC NCBI

Linked Data

dbSNP Id: rs2039230307

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80111202_80111203del , CM000679.2:g.80111202_80111203del GRCh38
NC_000017.10:g.78085001_78085002del , CM000679.1:g.78085001_78085002del GRCh37
NC_000017.9:g.75699596_75699597del NCBI36
NG_009822.1:g.14647_14648del , LRG_673:g.14647_14648del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1636+177_1636+178del ENSP00000460543.2:n.1636+177_1636+178del
ENST00000572080.2:c.1636+177_1636+178del ENSP00000459972.2:n.1636+177_1636+178del
ENST00000577106.6:c.1636+177_1636+178del ENSP00000458306.2:n.1636+177_1636+178del
ENST00000302262.8:c.1636+177_1636+178del MANE Select ENSP00000305692.3:n.1636+177_1636+178del
ENST00000302262.7:c.1636+177_1636+178del ENSP00000305692.3:n.1636+177_1636+178del
ENST00000390015.7:c.1636+177_1636+178del ENSP00000374665.3:n.1636+177_1636+178del
ENST00000572080.1:c.24+177_24+178del
NM_000152.3:c.1636+177_1636+178del , LRG_673t1:c.1636+177_1636+178del NP_000143.2:n.1636+177_1636+178del
NM_001079803.1:c.1636+177_1636+178del NP_001073271.1:n.1636+177_1636+178del
NM_001079804.1:c.1636+177_1636+178del NP_001073272.1:n.1636+177_1636+178del
XM_005257193.1:c.1636+177_1636+178del XP_005257250.1:n.1636+177_1636+178del
XM_005257194.3:c.1636+177_1636+178del XP_005257251.1:n.1636+177_1636+178del
NM_000152.4:c.1636+177_1636+178del NP_000143.2:n.1636+177_1636+178del
NM_001079803.2:c.1636+177_1636+178del NP_001073271.1:n.1636+177_1636+178del
NM_001079804.2:c.1636+177_1636+178del NP_001073272.1:n.1636+177_1636+178del
XM_005257193.2:c.1636+177_1636+178del XP_005257250.1:n.1636+177_1636+178del
XM_005257194.4:c.1636+177_1636+178del XP_005257251.1:n.1636+177_1636+178del
NM_000152.5:c.1636+177_1636+178del MANE Select NP_000143.2:n.1636+177_1636+178del
NM_001079803.3:c.1636+177_1636+178del NP_001073271.1:n.1636+177_1636+178del
NM_001079804.3:c.1636+177_1636+178del NP_001073272.1:n.1636+177_1636+178del