Canonical Allele Identifier: CA490587237

Gene: ALDH1A2

Linked Data

• gnomAD v4: 15-58010656-A-G
• MyVariant Identifiers: chr15:g.58302854A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010656A>G , CM000677.2:g.58010656A>G	GRCh38
NC_000015.9:g.58302854A>G , CM000677.1:g.58302854A>G	GRCh37
NC_000015.8:g.56090146A>G	NCBI36
NG_012259.1:g.60053T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.486T>C MANE Select	ENSP00000249750.4:p.Ile162=
ENST00000249750.8:c.486T>C	ENSP00000249750.4:p.Ile162=
ENST00000347587.7:c.486T>C	ENSP00000309623.3:p.Ile162=
ENST00000430119.6:c.*460T>C	ENSP00000416754.2:n.*460T>C
ENST00000537372.5:c.423T>C	ENSP00000438296.1:p.Ile141=
ENST00000558231.5:c.399T>C	ENSP00000453600.1:p.Ile133=
ENST00000559266.5:n.318+3202T>C
ENST00000559517.5:c.198T>C	ENSP00000453408.1:p.Ile66=
ENST00000561070.5:c.198T>C	ENSP00000452850.1:p.Ile66=
NM_001206897.1:c.423T>C	NP_001193826.1:p.Ile141=
NM_003888.3:c.486T>C	NP_003879.2:p.Ile162=
NM_170696.2:c.486T>C	NP_733797.1:p.Ile162=
NM_170697.2:c.198T>C	NP_733798.1:p.Ile66=
XM_024450095.1:c.486T>C	XP_024305863.1:p.Ile162=
NM_003888.4:c.486T>C MANE Select	NP_003879.2:p.Ile162=
NM_170696.3:c.486T>C	NP_733797.1:p.Ile162=
NM_170697.3:c.198T>C	NP_733798.1:p.Ile66=
NM_001206897.2:c.423T>C	NP_001193826.1:p.Ile141=