Canonical Allele Identifier: CA1141580623

Gene: ALDH4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.18877498G= , CM000663.2:g.18877498G=	GRCh38
NC_000001.10:g.19203992G= , CM000663.1:g.19203992G=	GRCh37
NC_000001.9:g.19076579G=	NCBI36
NG_012283.1:g.30302C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375341.8:c.1055C= MANE Select	ENSP00000364490.3:p.Ser352=
ENST00000290597.9:c.1055C=	ENSP00000290597.5:p.Ser352=
ENST00000375341.7:c.1055C=	ENSP00000364490.3:p.Ser352=
ENST00000494072.3:c.2107C=
ENST00000538309.5:c.875C=	ENSP00000442988.1:p.Ser292=
ENST00000538839.5:c.1055C=	ENSP00000446071.1:p.Ser352=
NM_001161504.1:c.875C=	NP_001154976.1:p.Ser292=
NM_003748.3:c.1055C=	NP_003739.2:p.Ser352=
NM_170726.2:c.1055C=	NP_733844.1:p.Ser352=
XM_011542352.1:c.1055C=	XP_011540654.1:p.Ser352=
XM_011542353.1:c.867C=	XP_011540655.1:p.Leu289=
XR_946786.1:n.924C=
NM_001319218.1:c.1055C=	NP_001306147.1:p.Ser352=
XR_001737510.1:n.924C=
NM_003748.4:c.1055C= MANE Select	NP_003739.2:p.Ser352=
NM_170726.3:c.1055C=	NP_733844.1:p.Ser352=
NM_001161504.2:c.875C=	NP_001154976.1:p.Ser292=
NM_001319218.2:c.1055C=	NP_001306147.1:p.Ser352=