Canonical Allele Identifier: CA1192431826
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119727078C= , CM000663.2:g.119727078C= GRCh38
NC_000001.10:g.120269701C= , CM000663.1:g.120269701C= GRCh37
NC_000001.9:g.120071224C= NCBI36
NG_009188.1:g.20283C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.486C= ENSP00000358417.5:p.Thr162=
ENST00000462324.2:n.569C=
ENST00000641023.2:c.486C= MANE Select ENSP00000493175.1:p.Thr162=
ENST00000641074.1:c.486C= ENSP00000493446.1:p.Thr162=
ENST00000641115.1:c.486C= ENSP00000493264.1:p.Thr162=
ENST00000641213.1:c.*139C= ENSP00000493079.1:n.*139C=
ENST00000641247.1:c.*205C= ENSP00000492955.1:n.*205C=
ENST00000641272.1:c.420C= ENSP00000493432.1:p.Thr140=
ENST00000641314.1:n.471C=
ENST00000641371.1:c.400C= ENSP00000493305.1:p.Pro134=
ENST00000641375.1:c.*322C= ENSP00000493089.1:n.*322C=
ENST00000641455.1:n.31C=
ENST00000641491.1:c.*139C= ENSP00000493187.1:n.*139C=
ENST00000641570.1:c.*205C= ENSP00000493213.1:n.*205C=
ENST00000641573.1:n.574C=
ENST00000641587.1:c.*197C= ENSP00000493453.1:n.*197C=
ENST00000641597.1:c.486C= ENSP00000493382.1:p.Thr162=
ENST00000641711.1:n.710C=
ENST00000641756.1:c.*230C= ENSP00000493147.1:n.*230C=
ENST00000641811.1:c.242C=
ENST00000641847.1:n.345C=
ENST00000641891.1:c.*312C= ENSP00000493288.1:n.*312C=
ENST00000641927.1:n.426C=
ENST00000641947.1:c.486C= ENSP00000492994.1:p.Thr162=
ENST00000642021.1:n.608C=
ENST00000369407.3:c.384C= ENSP00000358415.3:p.Thr128=
ENST00000369409.8:c.486C= ENSP00000358417.4:p.Thr162=
ENST00000462324.1:n.754C=
ENST00000493622.5:n.675C=
NM_006623.3:c.486C= NP_006614.2:p.Thr162=
XM_011541226.1:c.708C= XP_011539528.1:p.Thr236=
XM_011541227.1:c.630C= XP_011539529.1:p.Thr210=
XM_011541228.1:c.597C= XP_011539530.1:p.Thr199=
XM_011541229.1:c.423C= XP_011539531.1:p.Thr141=
XM_011541230.1:c.201C= XP_011539532.1:p.Thr67=
XM_011541231.1:c.192C= XP_011539533.1:p.Thr64=
XM_011541226.2:c.708C= XP_011539528.1:p.Thr236=
XM_011541227.2:c.630C= XP_011539529.1:p.Thr210=
XM_011541228.2:c.597C= XP_011539530.1:p.Thr199=
XM_011541231.2:c.192C= XP_011539533.1:p.Thr64=
XM_024446338.1:c.597C= XP_024302106.1:p.Thr199=
NM_006623.4:c.486C= MANE Select NP_006614.2:p.Thr162=