Canonical Allele Identifier: CA2628668924
Gene: ALDH1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58010614C>G , CM000677.2:g.58010614C>G GRCh38
NC_000015.9:g.58302812C>G , CM000677.1:g.58302812C>G GRCh37
NC_000015.8:g.56090104C>G NCBI36
NG_012259.1:g.60095G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000249750.9:c.493+35G>C MANE Select ENSP00000249750.4:n.493+35G>C
ENST00000249750.8:c.493+35G>C ENSP00000249750.4:n.493+35G>C
ENST00000347587.7:c.493+35G>C ENSP00000309623.3:n.493+35G>C
ENST00000430119.6:c.*467+35G>C ENSP00000416754.2:n.*467+35G>C
ENST00000537372.5:c.430+35G>C ENSP00000438296.1:n.430+35G>C
ENST00000558231.5:c.406+35G>C ENSP00000453600.1:n.406+35G>C
ENST00000559266.5:n.318+3244G>C
ENST00000559517.5:c.205+35G>C ENSP00000453408.1:n.205+35G>C
ENST00000561070.5:c.205+35G>C ENSP00000452850.1:n.205+35G>C
NM_001206897.1:c.430+35G>C NP_001193826.1:n.430+35G>C
NM_003888.3:c.493+35G>C NP_003879.2:n.493+35G>C
NM_170696.2:c.493+35G>C NP_733797.1:n.493+35G>C
NM_170697.2:c.205+35G>C NP_733798.1:n.205+35G>C
XM_024450095.1:c.493+35G>C XP_024305863.1:n.493+35G>C
NM_003888.4:c.493+35G>C MANE Select NP_003879.2:n.493+35G>C
NM_170696.3:c.493+35G>C NP_733797.1:n.493+35G>C
NM_170697.3:c.205+35G>C NP_733798.1:n.205+35G>C
NM_001206897.2:c.430+35G>C NP_001193826.1:n.430+35G>C