Canonical Allele Identifier: CA392789891

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302856T>C (hg19) ; chr15:g.58010658T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010658T>C , CM000677.2:g.58010658T>C	GRCh38
NC_000015.9:g.58302856T>C , CM000677.1:g.58302856T>C	GRCh37
NC_000015.8:g.56090148T>C	NCBI36
NG_012259.1:g.60051A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.484A>G MANE Select	ENSP00000249750.4:p.Ile162Val
ENST00000249750.8:c.484A>G	ENSP00000249750.4:p.Ile162Val
ENST00000347587.7:c.484A>G	ENSP00000309623.3:p.Ile162Val
ENST00000430119.6:c.*458A>G	ENSP00000416754.2:n.*458A>G
ENST00000537372.5:c.421A>G	ENSP00000438296.1:p.Ile141Val
ENST00000558231.5:c.397A>G	ENSP00000453600.1:p.Ile133Val
ENST00000559266.5:n.318+3200A>G
ENST00000559517.5:c.196A>G	ENSP00000453408.1:p.Ile66Val
ENST00000561070.5:c.196A>G	ENSP00000452850.1:p.Ile66Val
NM_001206897.1:c.421A>G	NP_001193826.1:p.Ile141Val
NM_003888.3:c.484A>G	NP_003879.2:p.Ile162Val
NM_170696.2:c.484A>G	NP_733797.1:p.Ile162Val
NM_170697.2:c.196A>G	NP_733798.1:p.Ile66Val
XM_024450095.1:c.484A>G	XP_024305863.1:p.Ile162Val
NM_003888.4:c.484A>G MANE Select	NP_003879.2:p.Ile162Val
NM_170696.3:c.484A>G	NP_733797.1:p.Ile162Val
NM_170697.3:c.196A>G	NP_733798.1:p.Ile66Val
NM_001206897.2:c.421A>G	NP_001193826.1:p.Ile141Val