Canonical Allele Identifier: CA392790196

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302931A>T (hg19) ; chr15:g.58010733A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010733A>T , CM000677.2:g.58010733A>T	GRCh38
NC_000015.9:g.58302931A>T , CM000677.1:g.58302931A>T	GRCh37
NC_000015.8:g.56090223A>T	NCBI36
NG_012259.1:g.59976T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.409T>A MANE Select	ENSP00000249750.4:p.Tyr137Asn
ENST00000249750.8:c.409T>A	ENSP00000249750.4:p.Tyr137Asn
ENST00000347587.7:c.409T>A	ENSP00000309623.3:p.Tyr137Asn
ENST00000430119.6:c.*383T>A	ENSP00000416754.2:n.*383T>A
ENST00000537372.5:c.346T>A	ENSP00000438296.1:p.Tyr116Asn
ENST00000558231.5:c.322T>A	ENSP00000453600.1:p.Tyr108Asn
ENST00000559266.5:n.318+3125T>A
ENST00000559517.5:c.121T>A	ENSP00000453408.1:p.Tyr41Asn
ENST00000561070.5:c.121T>A	ENSP00000452850.1:p.Tyr41Asn
NM_001206897.1:c.346T>A	NP_001193826.1:p.Tyr116Asn
NM_003888.3:c.409T>A	NP_003879.2:p.Tyr137Asn
NM_170696.2:c.409T>A	NP_733797.1:p.Tyr137Asn
NM_170697.2:c.121T>A	NP_733798.1:p.Tyr41Asn
XM_024450095.1:c.409T>A	XP_024305863.1:p.Tyr137Asn
NM_003888.4:c.409T>A MANE Select	NP_003879.2:p.Tyr137Asn
NM_170696.3:c.409T>A	NP_733797.1:p.Tyr137Asn
NM_170697.3:c.121T>A	NP_733798.1:p.Tyr41Asn
NM_001206897.2:c.346T>A	NP_001193826.1:p.Tyr116Asn