Canonical Allele Identifier: CA490587267

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302902G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010704G>T , CM000677.2:g.58010704G>T	GRCh38
NC_000015.9:g.58302902G>T , CM000677.1:g.58302902G>T	GRCh37
NC_000015.8:g.56090194G>T	NCBI36
NG_012259.1:g.60005C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.438C>A MANE Select	ENSP00000249750.4:p.Thr146=
ENST00000249750.8:c.438C>A	ENSP00000249750.4:p.Thr146=
ENST00000347587.7:c.438C>A	ENSP00000309623.3:p.Thr146=
ENST00000430119.6:c.*412C>A	ENSP00000416754.2:n.*412C>A
ENST00000537372.5:c.375C>A	ENSP00000438296.1:p.Thr125=
ENST00000558231.5:c.351C>A	ENSP00000453600.1:p.Thr117=
ENST00000559266.5:n.318+3154C>A
ENST00000559517.5:c.150C>A	ENSP00000453408.1:p.Thr50=
ENST00000561070.5:c.150C>A	ENSP00000452850.1:p.Thr50=
NM_001206897.1:c.375C>A	NP_001193826.1:p.Thr125=
NM_003888.3:c.438C>A	NP_003879.2:p.Thr146=
NM_170696.2:c.438C>A	NP_733797.1:p.Thr146=
NM_170697.2:c.150C>A	NP_733798.1:p.Thr50=
XM_024450095.1:c.438C>A	XP_024305863.1:p.Thr146=
NM_003888.4:c.438C>A MANE Select	NP_003879.2:p.Thr146=
NM_170696.3:c.438C>A	NP_733797.1:p.Thr146=
NM_170697.3:c.150C>A	NP_733798.1:p.Thr50=
NM_001206897.2:c.375C>A	NP_001193826.1:p.Thr125=