Canonical Allele Identifier: CA2574241456
Gene: ALDH4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.18902410T>A , CM000663.2:g.18902410T>A GRCh38
NC_000001.10:g.19228904T>A , CM000663.1:g.19228904T>A GRCh37
NC_000001.9:g.19101491T>A NCBI36
NG_012283.1:g.5390A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375341.8:c.62+52A>T MANE Select ENSP00000364490.3:n.62+52A>T
ENST00000290597.9:c.62+52A>T ENSP00000290597.5:n.62+52A>T
ENST00000375341.7:c.62+52A>T ENSP00000364490.3:n.62+52A>T
ENST00000432718.1:c.62+52A>T ENSP00000393209.1:n.62+52A>T
ENST00000494072.3:c.911+6129A>T
ENST00000538839.5:c.62+52A>T ENSP00000446071.1:n.62+52A>T
NM_003748.3:c.62+52A>T NP_003739.2:n.62+52A>T
NM_170726.2:c.62+52A>T NP_733844.1:n.62+52A>T
XM_011542352.1:c.62+52A>T XP_011540654.1:n.62+52A>T
XM_011542353.1:c.62+52A>T XP_011540655.1:n.62+52A>T
XR_946786.1:n.119+52A>T
NM_001319218.1:c.62+52A>T NP_001306147.1:n.62+52A>T
XR_001737510.1:n.119+52A>T
NM_003748.4:c.62+52A>T MANE Select NP_003739.2:n.62+52A>T
NM_170726.3:c.62+52A>T NP_733844.1:n.62+52A>T
NM_001319218.2:c.62+52A>T NP_001306147.1:n.62+52A>T