Canonical Allele Identifier: CA1140479552

Gene: ALDH4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.18879840G= , CM000663.2:g.18879840G=	GRCh38
NC_000001.10:g.19206334G= , CM000663.1:g.19206334G=	GRCh37
NC_000001.9:g.19078921G=	NCBI36
NG_012283.1:g.27960C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375341.8:c.867-467C= MANE Select	ENSP00000364490.3:n.867-467C=
ENST00000290597.9:c.867-467C=	ENSP00000290597.5:n.867-467C=
ENST00000375341.7:c.867-467C=	ENSP00000364490.3:n.867-467C=
ENST00000494072.3:c.1919-467C=
ENST00000538309.5:c.687-467C=	ENSP00000442988.1:n.687-467C=
ENST00000538839.5:c.867-467C=	ENSP00000446071.1:n.867-467C=
NM_001161504.1:c.687-467C=	NP_001154976.1:n.687-467C=
NM_003748.3:c.867-467C=	NP_003739.2:n.867-467C=
NM_170726.2:c.867-467C=	NP_733844.1:n.867-467C=
XM_011542352.1:c.867-467C=	XP_011540654.1:n.867-467C=
XM_011542353.1:c.679-467C=	XP_011540655.1:n.679-467C=
XR_946786.1:n.736-467C=
NM_001319218.1:c.867-467C=	NP_001306147.1:n.867-467C=
XR_001737510.1:n.736-467C=
NM_003748.4:c.867-467C= MANE Select	NP_003739.2:n.867-467C=
NM_170726.3:c.867-467C=	NP_733844.1:n.867-467C=
NM_001161504.2:c.687-467C=	NP_001154976.1:n.687-467C=
NM_001319218.2:c.867-467C=	NP_001306147.1:n.867-467C=