Canonical Allele Identifier: CA2277810783
Gene: GAA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80105021A= , CM000679.2:g.80105021A= GRCh38
NC_000017.10:g.78078820A= , CM000679.1:g.78078820A= GRCh37
NC_000017.9:g.75693415A= NCBI36
NG_009822.1:g.8466A= , LRG_673:g.8466A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.435A= ENSP00000460543.2:p.Glu145=
ENST00000572080.2:c.435A= ENSP00000459972.2:p.Glu145=
ENST00000577106.6:c.435A= ENSP00000458306.2:p.Glu145=
ENST00000302262.8:c.435A= MANE Select ENSP00000305692.3:p.Glu145=
ENST00000302262.7:c.435A= ENSP00000305692.3:p.Glu145=
ENST00000390015.7:c.435A= ENSP00000374665.3:p.Glu145=
ENST00000570803.5:c.435A= ENSP00000460543.1:p.Glu145=
ENST00000577106.5:c.435A= ENSP00000458306.1:p.Glu145=
NM_000152.3:c.435A= , LRG_673t1:c.435A= NP_000143.2:p.Glu145=
NM_001079803.1:c.435A= NP_001073271.1:p.Glu145=
NM_001079804.1:c.435A= NP_001073272.1:p.Glu145=
XM_005257193.1:c.435A= XP_005257250.1:p.Glu145=
XM_005257194.3:c.435A= XP_005257251.1:p.Glu145=
NM_000152.4:c.435A= NP_000143.2:p.Glu145=
NM_001079803.2:c.435A= NP_001073271.1:p.Glu145=
NM_001079804.2:c.435A= NP_001073272.1:p.Glu145=
XM_005257193.2:c.435A= XP_005257250.1:p.Glu145=
XM_005257194.4:c.435A= XP_005257251.1:p.Glu145=
NM_000152.5:c.435A= MANE Select NP_000143.2:p.Glu145=
NM_001079803.3:c.435A= NP_001073271.1:p.Glu145=
NM_001079804.3:c.435A= NP_001073272.1:p.Glu145=
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