Canonical Allele Identifier: CA2277809012

Gene: GAA

Linked Data

• dbSNP Id: rs2038949872

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80101620del , CM000679.2:g.80101620del	GRCh38
NC_000017.10:g.78075419del , CM000679.1:g.78075419del	GRCh37
NC_000017.9:g.75690014del	NCBI36
NG_009822.1:g.5065del , LRG_673:g.5065del
NG_029761.1:g.69989del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.-38del	ENSP00000460543.2:n.-38del
ENST00000572080.2:c.-118del	ENSP00000459972.2:n.-118del
ENST00000577106.6:c.-153del	ENSP00000458306.2:n.-153del
ENST00000302262.8:c.-303del MANE Select	ENSP00000305692.3:n.-303del
ENST00000390015.7:c.-118del	ENSP00000374665.3:n.-118del
ENST00000570803.5:c.-38del	ENSP00000460543.1:n.-38del
ENST00000574376.1:n.24del
ENST00000577106.5:c.-153del	ENSP00000458306.1:n.-153del
NM_000152.3:c.-303del , LRG_673t1:c.-303del	NP_000143.2:n.-303del
NM_001079803.1:c.-118del	NP_001073271.1:n.-118del
NM_001079804.1:c.-38del	NP_001073272.1:n.-38del
XM_005257193.1:c.-213del	XP_005257250.1:n.-213del
XM_005257194.3:c.-153del	XP_005257251.1:n.-153del
NM_000152.4:c.-303del	NP_000143.2:n.-303del
NM_001079803.2:c.-118del	NP_001073271.1:n.-118del
NM_001079804.2:c.-38del	NP_001073272.1:n.-38del
NR_134848.1:n.95del
XM_005257194.4:c.-153del	XP_005257251.1:n.-153del
NM_000152.5:c.-303del MANE Select	NP_000143.2:n.-303del
NM_001079803.3:c.-118del	NP_001073271.1:n.-118del
NM_001079804.3:c.-38del	NP_001073272.1:n.-38del
NR_134848.2:n.40del