Canonical Allele Identifier: CA2628669014
Gene: ALDH1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58010930C>A , CM000677.2:g.58010930C>A GRCh38
NC_000015.9:g.58303128C>A , CM000677.1:g.58303128C>A GRCh37
NC_000015.8:g.56090420C>A NCBI36
NG_012259.1:g.59779G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249750.9:c.364-152G>T MANE Select ENSP00000249750.4:n.364-152G>T
ENST00000249750.8:c.364-152G>T ENSP00000249750.4:n.364-152G>T
ENST00000347587.7:c.364-152G>T ENSP00000309623.3:n.364-152G>T
ENST00000430119.6:c.*338-152G>T ENSP00000416754.2:n.*338-152G>T
ENST00000537372.5:c.301-152G>T ENSP00000438296.1:n.301-152G>T
ENST00000558231.5:c.277-152G>T ENSP00000453600.1:n.277-152G>T
ENST00000559266.5:n.318+2928G>T
ENST00000559517.5:c.76-152G>T ENSP00000453408.1:n.76-152G>T
ENST00000561070.5:c.76-152G>T ENSP00000452850.1:n.76-152G>T
NM_001206897.1:c.301-152G>T NP_001193826.1:n.301-152G>T
NM_003888.3:c.364-152G>T NP_003879.2:n.364-152G>T
NM_170696.2:c.364-152G>T NP_733797.1:n.364-152G>T
NM_170697.2:c.76-152G>T NP_733798.1:n.76-152G>T
XM_024450095.1:c.364-152G>T XP_024305863.1:n.364-152G>T
NM_003888.4:c.364-152G>T MANE Select NP_003879.2:n.364-152G>T
NM_170696.3:c.364-152G>T NP_733797.1:n.364-152G>T
NM_170697.3:c.76-152G>T NP_733798.1:n.76-152G>T
NM_001206897.2:c.301-152G>T NP_001193826.1:n.301-152G>T