Canonical Allele Identifier: CA392790291
Gene: ALDH1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58010777G>C , CM000677.2:g.58010777G>C GRCh38
NC_000015.9:g.58302975G>C , CM000677.1:g.58302975G>C GRCh37
NC_000015.8:g.56090267G>C NCBI36
NG_012259.1:g.59932C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249750.9:c.365C>G MANE Select ENSP00000249750.4:p.Thr122Ser
ENST00000249750.8:c.365C>G ENSP00000249750.4:p.Thr122Ser
ENST00000347587.7:c.365C>G ENSP00000309623.3:p.Thr122Ser
ENST00000430119.6:c.*339C>G ENSP00000416754.2:n.*339C>G
ENST00000537372.5:c.302C>G ENSP00000438296.1:p.Thr101Ser
ENST00000558231.5:c.278C>G ENSP00000453600.1:p.Thr93Ser
ENST00000559266.5:n.318+3081C>G
ENST00000559517.5:c.77C>G ENSP00000453408.1:p.Thr26Ser
ENST00000561070.5:c.77C>G ENSP00000452850.1:p.Thr26Ser
NM_001206897.1:c.302C>G NP_001193826.1:p.Thr101Ser
NM_003888.3:c.365C>G NP_003879.2:p.Thr122Ser
NM_170696.2:c.365C>G NP_733797.1:p.Thr122Ser
NM_170697.2:c.77C>G NP_733798.1:p.Thr26Ser
XM_024450095.1:c.365C>G XP_024305863.1:p.Thr122Ser
NM_003888.4:c.365C>G MANE Select NP_003879.2:p.Thr122Ser
NM_170696.3:c.365C>G NP_733797.1:p.Thr122Ser
NM_170697.3:c.77C>G NP_733798.1:p.Thr26Ser
NM_001206897.2:c.302C>G NP_001193826.1:p.Thr101Ser