Canonical Allele Identifier: CA392789901

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302861A>G (hg19) ; chr15:g.58010663A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010663A>G , CM000677.2:g.58010663A>G	GRCh38
NC_000015.9:g.58302861A>G , CM000677.1:g.58302861A>G	GRCh37
NC_000015.8:g.56090153A>G	NCBI36
NG_012259.1:g.60046T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.479T>C MANE Select	ENSP00000249750.4:p.Met160Thr
ENST00000249750.8:c.479T>C	ENSP00000249750.4:p.Met160Thr
ENST00000347587.7:c.479T>C	ENSP00000309623.3:p.Met160Thr
ENST00000430119.6:c.*453T>C	ENSP00000416754.2:n.*453T>C
ENST00000537372.5:c.416T>C	ENSP00000438296.1:p.Met139Thr
ENST00000558231.5:c.392T>C	ENSP00000453600.1:p.Met131Thr
ENST00000559266.5:n.318+3195T>C
ENST00000559517.5:c.191T>C	ENSP00000453408.1:p.Met64Thr
ENST00000561070.5:c.191T>C	ENSP00000452850.1:p.Met64Thr
NM_001206897.1:c.416T>C	NP_001193826.1:p.Met139Thr
NM_003888.3:c.479T>C	NP_003879.2:p.Met160Thr
NM_170696.2:c.479T>C	NP_733797.1:p.Met160Thr
NM_170697.2:c.191T>C	NP_733798.1:p.Met64Thr
XM_024450095.1:c.479T>C	XP_024305863.1:p.Met160Thr
NM_003888.4:c.479T>C MANE Select	NP_003879.2:p.Met160Thr
NM_170696.3:c.479T>C	NP_733797.1:p.Met160Thr
NM_170697.3:c.191T>C	NP_733798.1:p.Met64Thr
NM_001206897.2:c.416T>C	NP_001193826.1:p.Met139Thr