Canonical Allele Identifier: CA647477

Gene: ALDH4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.18890029G>A , CM000663.2:g.18890029G>A	GRCh38
NC_000001.10:g.19216523G>A , CM000663.1:g.19216523G>A	GRCh37
NC_000001.9:g.19089110G>A	NCBI36
NG_012283.1:g.17771C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003748.4:c.139C>T MANE Select	NP_003739.2:p.Arg47Ter
ENST00000375341.8:c.139C>T MANE Select	ENSP00000364490.3:p.Arg47Ter
NM_001161504.1:c.-42C>T	NP_001154976.1:n.-42C>T
NM_001161504.2:c.-42C>T	NP_001154976.1:n.-42C>T
NM_001319218.1:c.139C>T	NP_001306147.1:p.Arg47Ter
NM_001319218.2:c.139C>T	NP_001306147.1:p.Arg47Ter
NM_003748.3:c.139C>T	NP_003739.2:p.Arg47Ter
NM_170726.2:c.139C>T	NP_733844.1:p.Arg47Ter
NM_170726.3:c.139C>T	NP_733844.1:p.Arg47Ter
ENST00000290597.9:c.139C>T	ENSP00000290597.5:p.Arg47Ter
ENST00000375341.7:c.139C>T	ENSP00000364490.3:p.Arg47Ter
ENST00000432718.1:c.139C>T	ENSP00000393209.1:p.Arg47Ter
ENST00000494072.3:c.1076C>T
ENST00000538309.5:c.-42C>T	ENSP00000442988.1:n.-42C>T
ENST00000538839.5:c.139C>T	ENSP00000446071.1:p.Arg47Ter
XM_011542352.1:c.139C>T	XP_011540654.1:p.Arg47Ter
XM_011542353.1:c.139C>T	XP_011540655.1:p.Arg47Ter
XR_001737510.1:n.196C>T
XR_946786.1:n.196C>T