Canonical Allele Identifier: CA2277810756
Gene: GAA HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80104969T= , CM000679.2:g.80104969T= GRCh38
NC_000017.10:g.78078768T= , CM000679.1:g.78078768T= GRCh37
NC_000017.9:g.75693363T= NCBI36
NG_009822.1:g.8414T= , LRG_673:g.8414T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.383T= ENSP00000460543.2:p.Phe128=
ENST00000572080.2:c.383T= ENSP00000459972.2:p.Phe128=
ENST00000577106.6:c.383T= ENSP00000458306.2:p.Phe128=
ENST00000302262.8:c.383T= MANE Select ENSP00000305692.3:p.Phe128=
ENST00000302262.7:c.383T= ENSP00000305692.3:p.Phe128=
ENST00000390015.7:c.383T= ENSP00000374665.3:p.Phe128=
ENST00000570803.5:c.383T= ENSP00000460543.1:p.Phe128=
ENST00000577106.5:c.383T= ENSP00000458306.1:p.Phe128=
NM_000152.3:c.383T= , LRG_673t1:c.383T= NP_000143.2:p.Phe128=
NM_001079803.1:c.383T= NP_001073271.1:p.Phe128=
NM_001079804.1:c.383T= NP_001073272.1:p.Phe128=
XM_005257193.1:c.383T= XP_005257250.1:p.Phe128=
XM_005257194.3:c.383T= XP_005257251.1:p.Phe128=
NM_000152.4:c.383T= NP_000143.2:p.Phe128=
NM_001079803.2:c.383T= NP_001073271.1:p.Phe128=
NM_001079804.2:c.383T= NP_001073272.1:p.Phe128=
XM_005257193.2:c.383T= XP_005257250.1:p.Phe128=
XM_005257194.4:c.383T= XP_005257251.1:p.Phe128=
NM_000152.5:c.383T= MANE Select NP_000143.2:p.Phe128=
NM_001079803.3:c.383T= NP_001073271.1:p.Phe128=
NM_001079804.3:c.383T= NP_001073272.1:p.Phe128=
Search 100 bp 5'
Search 100 bp 3'