Canonical Allele Identifier: CA1192431744
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119726893G= , CM000663.2:g.119726893G= GRCh38
NC_000001.10:g.120269516G= , CM000663.1:g.120269516G= GRCh37
NC_000001.9:g.120071039G= NCBI36
NG_009188.1:g.20098G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.399G= ENSP00000358417.5:p.Trp133=
ENST00000462324.2:n.482G=
ENST00000641023.2:c.399G= MANE Select ENSP00000493175.1:p.Trp133=
ENST00000641074.1:c.399G= ENSP00000493446.1:p.Trp133=
ENST00000641115.1:c.399G= ENSP00000493264.1:p.Trp133=
ENST00000641213.1:c.*52G= ENSP00000493079.1:n.*52G=
ENST00000641247.1:c.*118G= ENSP00000492955.1:n.*118G=
ENST00000641272.1:c.333G= ENSP00000493432.1:p.Trp111=
ENST00000641314.1:n.384G=
ENST00000641371.1:c.313G= ENSP00000493305.1:p.Gly105=
ENST00000641375.1:c.*235G= ENSP00000493089.1:n.*235G=
ENST00000641491.1:c.*52G= ENSP00000493187.1:n.*52G=
ENST00000641513.1:c.*143G= ENSP00000493398.1:n.*143G=
ENST00000641570.1:c.*118G= ENSP00000493213.1:n.*118G=
ENST00000641573.1:n.487G=
ENST00000641587.1:c.*110G= ENSP00000493453.1:n.*110G=
ENST00000641597.1:c.399G= ENSP00000493382.1:p.Trp133=
ENST00000641711.1:n.623G=
ENST00000641756.1:c.*143G= ENSP00000493147.1:n.*143G=
ENST00000641811.1:c.155G=
ENST00000641847.1:n.258G=
ENST00000641891.1:c.*225G= ENSP00000493288.1:n.*225G=
ENST00000641927.1:n.339G=
ENST00000641947.1:c.399G= ENSP00000492994.1:p.Trp133=
ENST00000642021.1:n.521G=
ENST00000642041.1:c.*438G= ENSP00000493415.1:n.*438G=
ENST00000369407.3:c.297G= ENSP00000358415.3:p.Trp99=
ENST00000369409.8:c.399G= ENSP00000358417.4:p.Trp133=
ENST00000462324.1:n.667G=
ENST00000493622.5:n.588G=
NM_006623.3:c.399G= NP_006614.2:p.Trp133=
XM_011541226.1:c.621G= XP_011539528.1:p.Trp207=
XM_011541227.1:c.543G= XP_011539529.1:p.Trp181=
XM_011541228.1:c.510G= XP_011539530.1:p.Trp170=
XM_011541229.1:c.336G= XP_011539531.1:p.Trp112=
XM_011541230.1:c.114G= XP_011539532.1:p.Trp38=
XM_011541231.1:c.105G= XP_011539533.1:p.Trp35=
XM_011541226.2:c.621G= XP_011539528.1:p.Trp207=
XM_011541227.2:c.543G= XP_011539529.1:p.Trp181=
XM_011541228.2:c.510G= XP_011539530.1:p.Trp170=
XM_011541231.2:c.105G= XP_011539533.1:p.Trp35=
XM_024446338.1:c.510G= XP_024302106.1:p.Trp170=
NM_006623.4:c.399G= MANE Select NP_006614.2:p.Trp133=