Canonical Allele Identifier: CA1192431738
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119726869G= , CM000663.2:g.119726869G= GRCh38
NC_000001.10:g.120269492G= , CM000663.1:g.120269492G= GRCh37
NC_000001.9:g.120071015G= NCBI36
NG_009188.1:g.20074G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.375G= ENSP00000358417.5:p.Thr125=
ENST00000462324.2:n.458G=
ENST00000641023.2:c.375G= MANE Select ENSP00000493175.1:p.Thr125=
ENST00000641074.1:c.375G= ENSP00000493446.1:p.Thr125=
ENST00000641115.1:c.375G= ENSP00000493264.1:p.Thr125=
ENST00000641213.1:c.*28G= ENSP00000493079.1:n.*28G=
ENST00000641247.1:c.*94G= ENSP00000492955.1:n.*94G=
ENST00000641272.1:c.309G= ENSP00000493432.1:p.Thr103=
ENST00000641314.1:n.360G=
ENST00000641371.1:c.289G= ENSP00000493305.1:p.Gly97=
ENST00000641375.1:c.*211G= ENSP00000493089.1:n.*211G=
ENST00000641491.1:c.*28G= ENSP00000493187.1:n.*28G=
ENST00000641513.1:c.*119G= ENSP00000493398.1:n.*119G=
ENST00000641570.1:c.*94G= ENSP00000493213.1:n.*94G=
ENST00000641573.1:n.463G=
ENST00000641587.1:c.*86G= ENSP00000493453.1:n.*86G=
ENST00000641597.1:c.375G= ENSP00000493382.1:p.Thr125=
ENST00000641711.1:n.599G=
ENST00000641756.1:c.*119G= ENSP00000493147.1:n.*119G=
ENST00000641811.1:c.131G=
ENST00000641847.1:n.234G=
ENST00000641891.1:c.*201G= ENSP00000493288.1:n.*201G=
ENST00000641927.1:n.315G=
ENST00000641947.1:c.375G= ENSP00000492994.1:p.Thr125=
ENST00000642021.1:n.497G=
ENST00000642041.1:c.*414G= ENSP00000493415.1:n.*414G=
ENST00000369407.3:c.273G= ENSP00000358415.3:p.Thr91=
ENST00000369409.8:c.375G= ENSP00000358417.4:p.Thr125=
ENST00000462324.1:n.643G=
ENST00000493622.5:n.564G=
NM_006623.3:c.375G= NP_006614.2:p.Thr125=
XM_011541226.1:c.597G= XP_011539528.1:p.Thr199=
XM_011541227.1:c.519G= XP_011539529.1:p.Thr173=
XM_011541228.1:c.486G= XP_011539530.1:p.Thr162=
XM_011541229.1:c.312G= XP_011539531.1:p.Thr104=
XM_011541230.1:c.90G= XP_011539532.1:p.Thr30=
XM_011541231.1:c.81G= XP_011539533.1:p.Thr27=
XM_011541226.2:c.597G= XP_011539528.1:p.Thr199=
XM_011541227.2:c.519G= XP_011539529.1:p.Thr173=
XM_011541228.2:c.486G= XP_011539530.1:p.Thr162=
XM_011541231.2:c.81G= XP_011539533.1:p.Thr27=
XM_024446338.1:c.486G= XP_024302106.1:p.Thr162=
NM_006623.4:c.375G= MANE Select NP_006614.2:p.Thr125=