Canonical Allele Identifier: CA338760636

Gene: ALDH4A1

Linked Data

• MyVariant Identifiers: chr1:g.19212051G>T (hg19) ; chr1:g.18885557G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.18885557G>T , CM000663.2:g.18885557G>T	GRCh38
NC_000001.10:g.19212051G>T , CM000663.1:g.19212051G>T	GRCh37
NC_000001.9:g.19084638G>T	NCBI36
NG_012283.1:g.22243C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375341.8:c.369C>A MANE Select	ENSP00000364490.3:p.Asp123Glu
ENST00000290597.9:c.369C>A	ENSP00000290597.5:p.Asp123Glu
ENST00000375341.7:c.369C>A	ENSP00000364490.3:p.Asp123Glu
ENST00000432718.1:c.321C>A	ENSP00000393209.1:p.Asp107Glu
ENST00000454547.1:n.63C>A
ENST00000494072.3:c.1306C>A
ENST00000538309.5:c.189C>A	ENSP00000442988.1:p.Asp63Glu
ENST00000538839.5:c.369C>A	ENSP00000446071.1:p.Asp123Glu
NM_001161504.1:c.189C>A	NP_001154976.1:p.Asp63Glu
NM_003748.3:c.369C>A	NP_003739.2:p.Asp123Glu
NM_170726.2:c.369C>A	NP_733844.1:p.Asp123Glu
XM_011542352.1:c.369C>A	XP_011540654.1:p.Asp123Glu
XM_011542353.1:c.369C>A	XP_011540655.1:p.Asp123Glu
XR_946786.1:n.426C>A
NM_001319218.1:c.369C>A	NP_001306147.1:p.Asp123Glu
XR_001737510.1:n.426C>A
NM_003748.4:c.369C>A MANE Select	NP_003739.2:p.Asp123Glu
NM_170726.3:c.369C>A	NP_733844.1:p.Asp123Glu
NM_001161504.2:c.189C>A	NP_001154976.1:p.Asp63Glu
NM_001319218.2:c.369C>A	NP_001306147.1:p.Asp123Glu