Canonical Allele Identifier: CA392790002

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302881C>T (hg19) ; chr15:g.58010683C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010683C>T , CM000677.2:g.58010683C>T	GRCh38
NC_000015.9:g.58302881C>T , CM000677.1:g.58302881C>T	GRCh37
NC_000015.8:g.56090173C>T	NCBI36
NG_012259.1:g.60026G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.459G>A MANE Select	ENSP00000249750.4:p.Trp153Ter
ENST00000249750.8:c.459G>A	ENSP00000249750.4:p.Trp153Ter
ENST00000347587.7:c.459G>A	ENSP00000309623.3:p.Trp153Ter
ENST00000430119.6:c.*433G>A	ENSP00000416754.2:n.*433G>A
ENST00000537372.5:c.396G>A	ENSP00000438296.1:p.Trp132Ter
ENST00000558231.5:c.372G>A	ENSP00000453600.1:p.Trp124Ter
ENST00000559266.5:n.318+3175G>A
ENST00000559517.5:c.171G>A	ENSP00000453408.1:p.Trp57Ter
ENST00000561070.5:c.171G>A	ENSP00000452850.1:p.Trp57Ter
NM_001206897.1:c.396G>A	NP_001193826.1:p.Trp132Ter
NM_003888.3:c.459G>A	NP_003879.2:p.Trp153Ter
NM_170696.2:c.459G>A	NP_733797.1:p.Trp153Ter
NM_170697.2:c.171G>A	NP_733798.1:p.Trp57Ter
XM_024450095.1:c.459G>A	XP_024305863.1:p.Trp153Ter
NM_003888.4:c.459G>A MANE Select	NP_003879.2:p.Trp153Ter
NM_170696.3:c.459G>A	NP_733797.1:p.Trp153Ter
NM_170697.3:c.171G>A	NP_733798.1:p.Trp57Ter
NM_001206897.2:c.396G>A	NP_001193826.1:p.Trp132Ter