Canonical Allele Identifier: CA2180084020

Gene: ALDH1A2

Linked Data

• dbSNP Id: rs1316790106

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.57987251A>G , CM000677.2:g.57987251A>G	GRCh38
NC_000015.9:g.58279449A>G , CM000677.1:g.58279449A>G	GRCh37
NC_000015.8:g.56066741A>G	NCBI36
NG_012259.1:g.83458T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000249750.9:c.798+5454T>C MANE Select	ENSP00000249750.4:n.798+5454T>C
ENST00000249750.8:c.798+5454T>C	ENSP00000249750.4:n.798+5454T>C
ENST00000347587.7:c.684+5694T>C	ENSP00000309623.3:n.684+5694T>C
ENST00000430119.6:c.*772+5454T>C	ENSP00000416754.2:n.*772+5454T>C
ENST00000537372.5:c.735+5454T>C	ENSP00000438296.1:n.735+5454T>C
ENST00000558231.5:c.711+5454T>C	ENSP00000453600.1:n.711+5454T>C
ENST00000559517.5:c.510+5454T>C	ENSP00000453408.1:n.510+5454T>C
NM_001206897.1:c.735+5454T>C	NP_001193826.1:n.735+5454T>C
NM_003888.3:c.798+5454T>C	NP_003879.2:n.798+5454T>C
NM_170696.2:c.684+5694T>C	NP_733797.1:n.684+5694T>C
NM_170697.2:c.510+5454T>C	NP_733798.1:n.510+5454T>C
NM_003888.4:c.798+5454T>C MANE Select	NP_003879.2:n.798+5454T>C
NM_170696.3:c.684+5694T>C	NP_733797.1:n.684+5694T>C
NM_170697.3:c.510+5454T>C	NP_733798.1:n.510+5454T>C
NM_001206897.2:c.735+5454T>C	NP_001193826.1:n.735+5454T>C