Canonical Allele Identifier: CA490587264

Gene: ALDH1A2

Linked Data

• gnomAD v4: 15-58010701-A-G
• MyVariant Identifiers: chr15:g.58302899A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010701A>G , CM000677.2:g.58010701A>G	GRCh38
NC_000015.9:g.58302899A>G , CM000677.1:g.58302899A>G	GRCh37
NC_000015.8:g.56090191A>G	NCBI36
NG_012259.1:g.60008T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000249750.9:c.441T>C MANE Select	ENSP00000249750.4:p.Phe147=
ENST00000249750.8:c.441T>C	ENSP00000249750.4:p.Phe147=
ENST00000347587.7:c.441T>C	ENSP00000309623.3:p.Phe147=
ENST00000430119.6:c.*415T>C	ENSP00000416754.2:n.*415T>C
ENST00000537372.5:c.378T>C	ENSP00000438296.1:p.Phe126=
ENST00000558231.5:c.354T>C	ENSP00000453600.1:p.Phe118=
ENST00000559266.5:n.318+3157T>C
ENST00000559517.5:c.153T>C	ENSP00000453408.1:p.Phe51=
ENST00000561070.5:c.153T>C	ENSP00000452850.1:p.Phe51=
NM_001206897.1:c.378T>C	NP_001193826.1:p.Phe126=
NM_003888.3:c.441T>C	NP_003879.2:p.Phe147=
NM_170696.2:c.441T>C	NP_733797.1:p.Phe147=
NM_170697.2:c.153T>C	NP_733798.1:p.Phe51=
XM_024450095.1:c.441T>C	XP_024305863.1:p.Phe147=
NM_003888.4:c.441T>C MANE Select	NP_003879.2:p.Phe147=
NM_170696.3:c.441T>C	NP_733797.1:p.Phe147=
NM_170697.3:c.153T>C	NP_733798.1:p.Phe51=
NM_001206897.2:c.378T>C	NP_001193826.1:p.Phe126=