Canonical Allele Identifier: CA126916169
Community Standard Title: NM_001182.5(ALDH7A1):c.332G>A (p.Gly111Glu)
Gene: ALDH7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126583993C>T , CM000667.2:g.126583993C>T GRCh38
NC_000005.9:g.125919685C>T , CM000667.1:g.125919685C>T GRCh37
NC_000005.8:g.125947584C>T NCBI36
NG_008600.2:g.16398G>A
NG_008600.3:g.16398G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001182.5:c.332G>A MANE Select NP_001173.2:p.Gly111Glu
ENST00000409134.8:c.332G>A MANE Select ENSP00000387123.3:p.Gly111Glu
NM_001182.4:c.332G>A NP_001173.2:p.Gly111Glu
NM_001201377.1:c.248G>A NP_001188306.1:p.Gly83Glu
NM_001201377.2:c.248G>A NP_001188306.1:p.Gly83Glu
NM_001202404.1:c.413G>A NP_001189333.1:p.Gly138Glu
NM_001202404.2:c.332G>A NP_001189333.2:p.Gly111Glu
ENST00000409134.7:c.332G>A ENSP00000387123.3:p.Gly111Glu
ENST00000412186.1:c.*141G>A ENSP00000414536.1:n.*141G>A
ENST00000412186.2:c.332G>A ENSP00000414536.2:p.Gly111Glu
ENST00000413020.5:c.332G>A ENSP00000487936.1:p.Gly111Glu
ENST00000413020.6:c.332G>A ENSP00000487936.1:p.Gly111Glu
ENST00000447989.6:c.413G>A ENSP00000414132.2:p.Gly138Glu
ENST00000458249.5:c.492G>A ENSP00000403929.1:n.492G>A
ENST00000458249.6:c.*241G>A ENSP00000403929.1:n.*241G>A
ENST00000479989.5:n.515G>A
ENST00000479989.6:n.515G>A
ENST00000503281.5:c.107-6782G>A
ENST00000503281.6:c.107-6782G>A
ENST00000509270.1:c.212G>A ENSP00000449318.1:p.Gly71Glu
ENST00000509270.2:c.266G>A ENSP00000449318.2:p.Gly89Glu
ENST00000509459.5:c.66-6782G>A
ENST00000509459.6:c.66-6782G>A
ENST00000510111.6:c.307-1019G>A ENSP00000447388.1:n.307-1019G>A
ENST00000511266.5:n.287G>A
ENST00000511266.6:n.1054G>A
ENST00000553117.5:c.332G>A ENSP00000448593.1:p.Gly111Glu
ENST00000635851.1:c.330G>A
ENST00000636062.1:n.227G>A
ENST00000636190.1:n.211G>A
ENST00000636225.1:c.*141G>A ENSP00000490797.1:n.*141G>A
ENST00000636286.1:n.50G>A
ENST00000636743.1:c.212G>A ENSP00000489725.1:p.Gly71Glu
ENST00000636808.1:c.*141G>A ENSP00000490833.1:n.*141G>A
ENST00000636872.1:c.492G>A ENSP00000490919.1:n.492G>A
ENST00000636879.1:c.332G>A ENSP00000490811.1:p.Gly111Glu
ENST00000636886.1:c.193-1019G>A ENSP00000490371.1:n.193-1019G>A
ENST00000637206.1:c.332G>A ENSP00000489895.1:p.Gly111Glu
ENST00000637272.1:c.332G>A ENSP00000489686.1:p.Gly111Glu
ENST00000637782.1:c.332G>A ENSP00000490024.1:p.Gly111Glu
ENST00000637964.1:c.278G>A ENSP00000490291.1:p.Gly93Glu
ENST00000638008.1:c.*274G>A ENSP00000490400.1:n.*274G>A
XM_011543417.1:c.-74G>A XP_011541719.1:n.-74G>A
XM_011543417.2:c.-74G>A XP_011541719.1:n.-74G>A