Canonical Allele Identifier: CA392790212
Gene: ALDH1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58010741T>A , CM000677.2:g.58010741T>A GRCh38
NC_000015.9:g.58302939T>A , CM000677.1:g.58302939T>A GRCh37
NC_000015.8:g.56090231T>A NCBI36
NG_012259.1:g.59968A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249750.9:c.401A>T MANE Select ENSP00000249750.4:p.Gln134Leu
ENST00000249750.8:c.401A>T ENSP00000249750.4:p.Gln134Leu
ENST00000347587.7:c.401A>T ENSP00000309623.3:p.Gln134Leu
ENST00000430119.6:c.*375A>T ENSP00000416754.2:n.*375A>T
ENST00000537372.5:c.338A>T ENSP00000438296.1:p.Gln113Leu
ENST00000558231.5:c.314A>T ENSP00000453600.1:p.Gln105Leu
ENST00000559266.5:n.318+3117A>T
ENST00000559517.5:c.113A>T ENSP00000453408.1:p.Gln38Leu
ENST00000561070.5:c.113A>T ENSP00000452850.1:p.Gln38Leu
NM_001206897.1:c.338A>T NP_001193826.1:p.Gln113Leu
NM_003888.3:c.401A>T NP_003879.2:p.Gln134Leu
NM_170696.2:c.401A>T NP_733797.1:p.Gln134Leu
NM_170697.2:c.113A>T NP_733798.1:p.Gln38Leu
XM_024450095.1:c.401A>T XP_024305863.1:p.Gln134Leu
NM_003888.4:c.401A>T MANE Select NP_003879.2:p.Gln134Leu
NM_170696.3:c.401A>T NP_733797.1:p.Gln134Leu
NM_170697.3:c.113A>T NP_733798.1:p.Gln38Leu
NM_001206897.2:c.338A>T NP_001193826.1:p.Gln113Leu