Canonical Allele Identifier: CA392789925
Gene: ALDH1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58010669T>A , CM000677.2:g.58010669T>A GRCh38
NC_000015.9:g.58302867T>A , CM000677.1:g.58302867T>A GRCh37
NC_000015.8:g.56090159T>A NCBI36
NG_012259.1:g.60040A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249750.9:c.473A>T MANE Select ENSP00000249750.4:p.His158Leu
ENST00000249750.8:c.473A>T ENSP00000249750.4:p.His158Leu
ENST00000347587.7:c.473A>T ENSP00000309623.3:p.His158Leu
ENST00000430119.6:c.*447A>T ENSP00000416754.2:n.*447A>T
ENST00000537372.5:c.410A>T ENSP00000438296.1:p.His137Leu
ENST00000558231.5:c.386A>T ENSP00000453600.1:p.His129Leu
ENST00000559266.5:n.318+3189A>T
ENST00000559517.5:c.185A>T ENSP00000453408.1:p.His62Leu
ENST00000561070.5:c.185A>T ENSP00000452850.1:p.His62Leu
NM_001206897.1:c.410A>T NP_001193826.1:p.His137Leu
NM_003888.3:c.473A>T NP_003879.2:p.His158Leu
NM_170696.2:c.473A>T NP_733797.1:p.His158Leu
NM_170697.2:c.185A>T NP_733798.1:p.His62Leu
XM_024450095.1:c.473A>T XP_024305863.1:p.His158Leu
NM_003888.4:c.473A>T MANE Select NP_003879.2:p.His158Leu
NM_170696.3:c.473A>T NP_733797.1:p.His158Leu
NM_170697.3:c.185A>T NP_733798.1:p.His62Leu
NM_001206897.2:c.410A>T NP_001193826.1:p.His137Leu