Canonical Allele Identifier: CA1144228700
Gene: ALDH4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.18902503C= , CM000663.2:g.18902503C= GRCh38
NC_000001.10:g.19228997C= , CM000663.1:g.19228997C= GRCh37
NC_000001.9:g.19101584C= NCBI36
NG_012283.1:g.5297G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375341.8:c.21G= MANE Select ENSP00000364490.3:p.Ala7=
ENST00000290597.9:c.21G= ENSP00000290597.5:p.Ala7=
ENST00000375341.7:c.21G= ENSP00000364490.3:p.Ala7=
ENST00000432718.1:c.21G= ENSP00000393209.1:p.Ala7=
ENST00000494072.3:c.911+6036G=
ENST00000538839.5:c.21G= ENSP00000446071.1:p.Ala7=
NM_003748.3:c.21G= NP_003739.2:p.Ala7=
NM_170726.2:c.21G= NP_733844.1:p.Ala7=
XM_011542352.1:c.21G= XP_011540654.1:p.Ala7=
XM_011542353.1:c.21G= XP_011540655.1:p.Ala7=
XR_946786.1:n.78G=
NM_001319218.1:c.21G= NP_001306147.1:p.Ala7=
XR_001737510.1:n.78G=
NM_003748.4:c.21G= MANE Select NP_003739.2:p.Ala7=
NM_170726.3:c.21G= NP_733844.1:p.Ala7=
NM_001319218.2:c.21G= NP_001306147.1:p.Ala7=