Canonical Allele Identifier: CA3227603051
Community Standard Title: NM_000152.5(GAA):c.587A= (p.Glu196=)
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80105789A= , CM000679.2:g.80105789A= GRCh38
NC_000017.10:g.78079588A= , CM000679.1:g.78079588A= GRCh37
NC_000017.9:g.75694183A= NCBI36
NG_009822.1:g.9234A= , LRG_673:g.9234A=

Transcript Alleles

HGVS Amino-acid Change
NM_000152.5:c.587A= MANE Select NP_000143.2:p.Glu196=
ENST00000302262.8:c.587A= MANE Select ENSP00000305692.3:p.Glu196=
NM_000152.3:c.587A= , LRG_673t1:c.587A= NP_000143.2:p.Glu196=
NM_000152.4:c.587A= NP_000143.2:p.Glu196=
NM_001079803.1:c.587A= NP_001073271.1:p.Glu196=
NM_001079803.2:c.587A= NP_001073271.1:p.Glu196=
NM_001079803.3:c.587A= NP_001073271.1:p.Glu196=
NM_001079804.1:c.587A= NP_001073272.1:p.Glu196=
NM_001079804.2:c.587A= NP_001073272.1:p.Glu196=
NM_001079804.3:c.587A= NP_001073272.1:p.Glu196=
ENST00000302262.7:c.587A= ENSP00000305692.3:p.Glu196=
ENST00000390015.7:c.587A= ENSP00000374665.3:p.Glu196=
ENST00000570803.5:c.587A= ENSP00000460543.1:p.Glu196=
ENST00000570803.6:c.587A= ENSP00000460543.2:p.Glu196=
ENST00000572080.2:c.587A= ENSP00000459972.2:p.Glu196=
ENST00000577106.5:c.587A= ENSP00000458306.1:p.Glu196=
ENST00000577106.6:c.587A= ENSP00000458306.2:p.Glu196=
XM_005257193.1:c.587A= XP_005257250.1:p.Glu196=
XM_005257193.2:c.587A= XP_005257250.1:p.Glu196=
XM_005257194.3:c.587A= XP_005257251.1:p.Glu196=
XM_005257194.4:c.587A= XP_005257251.1:p.Glu196=