Canonical Allele Identifier: CA392790073

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302894T>G (hg19) ; chr15:g.58010696T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010696T>G , CM000677.2:g.58010696T>G	GRCh38
NC_000015.9:g.58302894T>G , CM000677.1:g.58302894T>G	GRCh37
NC_000015.8:g.56090186T>G	NCBI36
NG_012259.1:g.60013A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.446A>C MANE Select	ENSP00000249750.4:p.Tyr149Ser
ENST00000249750.8:c.446A>C	ENSP00000249750.4:p.Tyr149Ser
ENST00000347587.7:c.446A>C	ENSP00000309623.3:p.Tyr149Ser
ENST00000430119.6:c.*420A>C	ENSP00000416754.2:n.*420A>C
ENST00000537372.5:c.383A>C	ENSP00000438296.1:p.Tyr128Ser
ENST00000558231.5:c.359A>C	ENSP00000453600.1:p.Tyr120Ser
ENST00000559266.5:n.318+3162A>C
ENST00000559517.5:c.158A>C	ENSP00000453408.1:p.Tyr53Ser
ENST00000561070.5:c.158A>C	ENSP00000452850.1:p.Tyr53Ser
NM_001206897.1:c.383A>C	NP_001193826.1:p.Tyr128Ser
NM_003888.3:c.446A>C	NP_003879.2:p.Tyr149Ser
NM_170696.2:c.446A>C	NP_733797.1:p.Tyr149Ser
NM_170697.2:c.158A>C	NP_733798.1:p.Tyr53Ser
XM_024450095.1:c.446A>C	XP_024305863.1:p.Tyr149Ser
NM_003888.4:c.446A>C MANE Select	NP_003879.2:p.Tyr149Ser
NM_170696.3:c.446A>C	NP_733797.1:p.Tyr149Ser
NM_170697.3:c.158A>C	NP_733798.1:p.Tyr53Ser
NM_001206897.2:c.383A>C	NP_001193826.1:p.Tyr128Ser