Canonical Allele Identifier: CA2180113982
Gene: ALDH1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58010604G= , CM000677.2:g.58010604G= GRCh38
NC_000015.9:g.58302802G= , CM000677.1:g.58302802G= GRCh37
NC_000015.8:g.56090094G= NCBI36
NG_012259.1:g.60105C=

Transcript Alleles

HGVS Amino-acid change
ENST00000249750.9:c.493+45C= MANE Select ENSP00000249750.4:n.493+45C=
ENST00000249750.8:c.493+45C= ENSP00000249750.4:n.493+45C=
ENST00000347587.7:c.493+45C= ENSP00000309623.3:n.493+45C=
ENST00000430119.6:c.*467+45C= ENSP00000416754.2:n.*467+45C=
ENST00000537372.5:c.430+45C= ENSP00000438296.1:n.430+45C=
ENST00000558231.5:c.406+45C= ENSP00000453600.1:n.406+45C=
ENST00000559266.5:n.318+3254C=
ENST00000559517.5:c.205+45C= ENSP00000453408.1:n.205+45C=
ENST00000561070.5:c.205+45C= ENSP00000452850.1:n.205+45C=
NM_001206897.1:c.430+45C= NP_001193826.1:n.430+45C=
NM_003888.3:c.493+45C= NP_003879.2:n.493+45C=
NM_170696.2:c.493+45C= NP_733797.1:n.493+45C=
NM_170697.2:c.205+45C= NP_733798.1:n.205+45C=
XM_024450095.1:c.493+45C= XP_024305863.1:n.493+45C=
NM_003888.4:c.493+45C= MANE Select NP_003879.2:n.493+45C=
NM_170696.3:c.493+45C= NP_733797.1:n.493+45C=
NM_170697.3:c.205+45C= NP_733798.1:n.205+45C=
NM_001206897.2:c.430+45C= NP_001193826.1:n.430+45C=