Canonical Allele Identifier: CA2180114076
Gene: ALDH1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58010692G= , CM000677.2:g.58010692G= GRCh38
NC_000015.9:g.58302890G= , CM000677.1:g.58302890G= GRCh37
NC_000015.8:g.56090182G= NCBI36
NG_012259.1:g.60017C=

Transcript Alleles

HGVS Amino-acid change
ENST00000249750.9:c.450C= MANE Select ENSP00000249750.4:p.Tyr150=
ENST00000249750.8:c.450C= ENSP00000249750.4:p.Tyr150=
ENST00000347587.7:c.450C= ENSP00000309623.3:p.Tyr150=
ENST00000430119.6:c.*424C= ENSP00000416754.2:n.*424C=
ENST00000537372.5:c.387C= ENSP00000438296.1:p.Tyr129=
ENST00000558231.5:c.363C= ENSP00000453600.1:p.Tyr121=
ENST00000559266.5:n.318+3166C=
ENST00000559517.5:c.162C= ENSP00000453408.1:p.Tyr54=
ENST00000561070.5:c.162C= ENSP00000452850.1:p.Tyr54=
NM_001206897.1:c.387C= NP_001193826.1:p.Tyr129=
NM_003888.3:c.450C= NP_003879.2:p.Tyr150=
NM_170696.2:c.450C= NP_733797.1:p.Tyr150=
NM_170697.2:c.162C= NP_733798.1:p.Tyr54=
XM_024450095.1:c.450C= XP_024305863.1:p.Tyr150=
NM_003888.4:c.450C= MANE Select NP_003879.2:p.Tyr150=
NM_170696.3:c.450C= NP_733797.1:p.Tyr150=
NM_170697.3:c.162C= NP_733798.1:p.Tyr54=
NM_001206897.2:c.387C= NP_001193826.1:p.Tyr129=