Canonical Allele Identifier: CA1141911554
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119727019C= , CM000663.2:g.119727019C= GRCh38
NC_000001.10:g.120269642C= , CM000663.1:g.120269642C= GRCh37
NC_000001.9:g.120071165C= NCBI36
NG_009188.1:g.20224C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.427C= ENSP00000358417.5:p.Leu143=
ENST00000462324.2:n.510C=
ENST00000641023.2:c.427C= MANE Select ENSP00000493175.1:p.Leu143=
ENST00000641074.1:c.427C= ENSP00000493446.1:p.Leu143=
ENST00000641115.1:c.427C= ENSP00000493264.1:p.Leu143=
ENST00000641213.1:c.*80C= ENSP00000493079.1:n.*80C=
ENST00000641247.1:c.*146C= ENSP00000492955.1:n.*146C=
ENST00000641272.1:c.361C= ENSP00000493432.1:p.Leu121=
ENST00000641314.1:n.412C=
ENST00000641371.1:c.341C= ENSP00000493305.1:p.Ala114=
ENST00000641375.1:c.*263C= ENSP00000493089.1:n.*263C=
ENST00000641491.1:c.*80C= ENSP00000493187.1:n.*80C=
ENST00000641570.1:c.*146C= ENSP00000493213.1:n.*146C=
ENST00000641573.1:n.515C=
ENST00000641587.1:c.*138C= ENSP00000493453.1:n.*138C=
ENST00000641597.1:c.427C= ENSP00000493382.1:p.Leu143=
ENST00000641711.1:n.651C=
ENST00000641756.1:c.*171C= ENSP00000493147.1:n.*171C=
ENST00000641811.1:c.183C=
ENST00000641847.1:n.286C=
ENST00000641891.1:c.*253C= ENSP00000493288.1:n.*253C=
ENST00000641927.1:n.367C=
ENST00000641947.1:c.427C= ENSP00000492994.1:p.Leu143=
ENST00000642021.1:n.549C=
ENST00000642041.1:c.*466C= ENSP00000493415.1:n.*466C=
ENST00000369407.3:c.325C= ENSP00000358415.3:p.Leu109=
ENST00000369409.8:c.427C= ENSP00000358417.4:p.Leu143=
ENST00000462324.1:n.695C=
ENST00000493622.5:n.616C=
NM_006623.3:c.427C= NP_006614.2:p.Leu143=
XM_011541226.1:c.649C= XP_011539528.1:p.Leu217=
XM_011541227.1:c.571C= XP_011539529.1:p.Leu191=
XM_011541228.1:c.538C= XP_011539530.1:p.Leu180=
XM_011541229.1:c.364C= XP_011539531.1:p.Leu122=
XM_011541230.1:c.142C= XP_011539532.1:p.Leu48=
XM_011541231.1:c.133C= XP_011539533.1:p.Leu45=
XM_011541226.2:c.649C= XP_011539528.1:p.Leu217=
XM_011541227.2:c.571C= XP_011539529.1:p.Leu191=
XM_011541228.2:c.538C= XP_011539530.1:p.Leu180=
XM_011541231.2:c.133C= XP_011539533.1:p.Leu45=
XM_024446338.1:c.538C= XP_024302106.1:p.Leu180=
NM_006623.4:c.427C= MANE Select NP_006614.2:p.Leu143=