Canonical Allele Identifier: CA490587256

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302884G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010686G>C , CM000677.2:g.58010686G>C	GRCh38
NC_000015.9:g.58302884G>C , CM000677.1:g.58302884G>C	GRCh37
NC_000015.8:g.56090176G>C	NCBI36
NG_012259.1:g.60023C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.456C>G MANE Select	ENSP00000249750.4:p.Gly152=
ENST00000249750.8:c.456C>G	ENSP00000249750.4:p.Gly152=
ENST00000347587.7:c.456C>G	ENSP00000309623.3:p.Gly152=
ENST00000430119.6:c.*430C>G	ENSP00000416754.2:n.*430C>G
ENST00000537372.5:c.393C>G	ENSP00000438296.1:p.Gly131=
ENST00000558231.5:c.369C>G	ENSP00000453600.1:p.Gly123=
ENST00000559266.5:n.318+3172C>G
ENST00000559517.5:c.168C>G	ENSP00000453408.1:p.Gly56=
ENST00000561070.5:c.168C>G	ENSP00000452850.1:p.Gly56=
NM_001206897.1:c.393C>G	NP_001193826.1:p.Gly131=
NM_003888.3:c.456C>G	NP_003879.2:p.Gly152=
NM_170696.2:c.456C>G	NP_733797.1:p.Gly152=
NM_170697.2:c.168C>G	NP_733798.1:p.Gly56=
XM_024450095.1:c.456C>G	XP_024305863.1:p.Gly152=
NM_003888.4:c.456C>G MANE Select	NP_003879.2:p.Gly152=
NM_170696.3:c.456C>G	NP_733797.1:p.Gly152=
NM_170697.3:c.168C>G	NP_733798.1:p.Gly56=
NM_001206897.2:c.393C>G	NP_001193826.1:p.Gly131=