Canonical Allele Identifier: CA1192431816
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119727053G= , CM000663.2:g.119727053G= GRCh38
NC_000001.10:g.120269676G= , CM000663.1:g.120269676G= GRCh37
NC_000001.9:g.120071199G= NCBI36
NG_009188.1:g.20258G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.461G= ENSP00000358417.5:p.Gly154=
ENST00000462324.2:n.544G=
ENST00000641023.2:c.461G= MANE Select ENSP00000493175.1:p.Gly154=
ENST00000641074.1:c.461G= ENSP00000493446.1:p.Gly154=
ENST00000641115.1:c.461G= ENSP00000493264.1:p.Gly154=
ENST00000641213.1:c.*114G= ENSP00000493079.1:n.*114G=
ENST00000641247.1:c.*180G= ENSP00000492955.1:n.*180G=
ENST00000641272.1:c.395G= ENSP00000493432.1:p.Gly132=
ENST00000641314.1:n.446G=
ENST00000641371.1:c.375G= ENSP00000493305.1:p.Gly125=
ENST00000641375.1:c.*297G= ENSP00000493089.1:n.*297G=
ENST00000641455.1:n.6G=
ENST00000641491.1:c.*114G= ENSP00000493187.1:n.*114G=
ENST00000641570.1:c.*180G= ENSP00000493213.1:n.*180G=
ENST00000641573.1:n.549G=
ENST00000641587.1:c.*172G= ENSP00000493453.1:n.*172G=
ENST00000641597.1:c.461G= ENSP00000493382.1:p.Gly154=
ENST00000641711.1:n.685G=
ENST00000641756.1:c.*205G= ENSP00000493147.1:n.*205G=
ENST00000641811.1:c.217G=
ENST00000641847.1:n.320G=
ENST00000641891.1:c.*287G= ENSP00000493288.1:n.*287G=
ENST00000641927.1:n.401G=
ENST00000641947.1:c.461G= ENSP00000492994.1:p.Gly154=
ENST00000642021.1:n.583G=
ENST00000642041.1:c.*500G= ENSP00000493415.1:n.*500G=
ENST00000369407.3:c.359G= ENSP00000358415.3:p.Gly120=
ENST00000369409.8:c.461G= ENSP00000358417.4:p.Gly154=
ENST00000462324.1:n.729G=
ENST00000493622.5:n.650G=
NM_006623.3:c.461G= NP_006614.2:p.Gly154=
XM_011541226.1:c.683G= XP_011539528.1:p.Gly228=
XM_011541227.1:c.605G= XP_011539529.1:p.Gly202=
XM_011541228.1:c.572G= XP_011539530.1:p.Gly191=
XM_011541229.1:c.398G= XP_011539531.1:p.Gly133=
XM_011541230.1:c.176G= XP_011539532.1:p.Gly59=
XM_011541231.1:c.167G= XP_011539533.1:p.Gly56=
XM_011541226.2:c.683G= XP_011539528.1:p.Gly228=
XM_011541227.2:c.605G= XP_011539529.1:p.Gly202=
XM_011541228.2:c.572G= XP_011539530.1:p.Gly191=
XM_011541231.2:c.167G= XP_011539533.1:p.Gly56=
XM_024446338.1:c.572G= XP_024302106.1:p.Gly191=
NM_006623.4:c.461G= MANE Select NP_006614.2:p.Gly154=