Canonical Allele Identifier: CA392789947

Gene: ALDH1A2

Linked Data

• dbSNP Id: rs2140514307
• MyVariant Identifiers: chr15:g.58302871T>C (hg19) ; chr15:g.58010673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010673T>C , CM000677.2:g.58010673T>C	GRCh38
NC_000015.9:g.58302871T>C , CM000677.1:g.58302871T>C	GRCh37
NC_000015.8:g.56090163T>C	NCBI36
NG_012259.1:g.60036A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.469A>G MANE Select	ENSP00000249750.4:p.Ile157Val
ENST00000249750.8:c.469A>G	ENSP00000249750.4:p.Ile157Val
ENST00000347587.7:c.469A>G	ENSP00000309623.3:p.Ile157Val
ENST00000430119.6:c.*443A>G	ENSP00000416754.2:n.*443A>G
ENST00000537372.5:c.406A>G	ENSP00000438296.1:p.Ile136Val
ENST00000558231.5:c.382A>G	ENSP00000453600.1:p.Ile128Val
ENST00000559266.5:n.318+3185A>G
ENST00000559517.5:c.181A>G	ENSP00000453408.1:p.Ile61Val
ENST00000561070.5:c.181A>G	ENSP00000452850.1:p.Ile61Val
NM_001206897.1:c.406A>G	NP_001193826.1:p.Ile136Val
NM_003888.3:c.469A>G	NP_003879.2:p.Ile157Val
NM_170696.2:c.469A>G	NP_733797.1:p.Ile157Val
NM_170697.2:c.181A>G	NP_733798.1:p.Ile61Val
XM_024450095.1:c.469A>G	XP_024305863.1:p.Ile157Val
NM_003888.4:c.469A>G MANE Select	NP_003879.2:p.Ile157Val
NM_170696.3:c.469A>G	NP_733797.1:p.Ile157Val
NM_170697.3:c.181A>G	NP_733798.1:p.Ile61Val
NM_001206897.2:c.406A>G	NP_001193826.1:p.Ile136Val