Canonical Allele Identifier: CA392790038

Gene: ALDH1A2

Linked Data

• dbSNP Id: rs115875978
• gnomAD v2: 15-58302889-C-T
• gnomAD v4: 15-58010691-C-T
• MyVariant Identifiers: chr15:g.58302889C>T (hg19) ; chr15:g.58010691C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010691C>T , CM000677.2:g.58010691C>T	GRCh38
NC_000015.9:g.58302889C>T , CM000677.1:g.58302889C>T	GRCh37
NC_000015.8:g.56090181C>T	NCBI36
NG_012259.1:g.60018G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000249750.9:c.451G>A MANE Select	ENSP00000249750.4:p.Ala151Thr
ENST00000249750.8:c.451G>A	ENSP00000249750.4:p.Ala151Thr
ENST00000347587.7:c.451G>A	ENSP00000309623.3:p.Ala151Thr
ENST00000430119.6:c.*425G>A	ENSP00000416754.2:n.*425G>A
ENST00000537372.5:c.388G>A	ENSP00000438296.1:p.Ala130Thr
ENST00000558231.5:c.364G>A	ENSP00000453600.1:p.Ala122Thr
ENST00000559266.5:n.318+3167G>A
ENST00000559517.5:c.163G>A	ENSP00000453408.1:p.Ala55Thr
ENST00000561070.5:c.163G>A	ENSP00000452850.1:p.Ala55Thr
NM_001206897.1:c.388G>A	NP_001193826.1:p.Ala130Thr
NM_003888.3:c.451G>A	NP_003879.2:p.Ala151Thr
NM_170696.2:c.451G>A	NP_733797.1:p.Ala151Thr
NM_170697.2:c.163G>A	NP_733798.1:p.Ala55Thr
XM_024450095.1:c.451G>A	XP_024305863.1:p.Ala151Thr
NM_003888.4:c.451G>A MANE Select	NP_003879.2:p.Ala151Thr
NM_170696.3:c.451G>A	NP_733797.1:p.Ala151Thr
NM_170697.3:c.163G>A	NP_733798.1:p.Ala55Thr
NM_001206897.2:c.388G>A	NP_001193826.1:p.Ala130Thr