Canonical Allele Identifier: CA1143391494
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119727014C= , CM000663.2:g.119727014C= GRCh38
NC_000001.10:g.120269637C= , CM000663.1:g.120269637C= GRCh37
NC_000001.9:g.120071160C= NCBI36
NG_009188.1:g.20219C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.422C= ENSP00000358417.5:p.Thr141=
ENST00000462324.2:n.505C=
ENST00000641023.2:c.422C= MANE Select ENSP00000493175.1:p.Thr141=
ENST00000641074.1:c.422C= ENSP00000493446.1:p.Thr141=
ENST00000641115.1:c.422C= ENSP00000493264.1:p.Thr141=
ENST00000641213.1:c.*75C= ENSP00000493079.1:n.*75C=
ENST00000641247.1:c.*141C= ENSP00000492955.1:n.*141C=
ENST00000641272.1:c.356C= ENSP00000493432.1:p.Thr119=
ENST00000641314.1:n.407C=
ENST00000641371.1:c.336C= ENSP00000493305.1:p.Asn112=
ENST00000641375.1:c.*258C= ENSP00000493089.1:n.*258C=
ENST00000641491.1:c.*75C= ENSP00000493187.1:n.*75C=
ENST00000641570.1:c.*141C= ENSP00000493213.1:n.*141C=
ENST00000641573.1:n.510C=
ENST00000641587.1:c.*133C= ENSP00000493453.1:n.*133C=
ENST00000641597.1:c.422C= ENSP00000493382.1:p.Thr141=
ENST00000641711.1:n.646C=
ENST00000641756.1:c.*166C= ENSP00000493147.1:n.*166C=
ENST00000641811.1:c.178C=
ENST00000641847.1:n.281C=
ENST00000641891.1:c.*248C= ENSP00000493288.1:n.*248C=
ENST00000641927.1:n.362C=
ENST00000641947.1:c.422C= ENSP00000492994.1:p.Thr141=
ENST00000642021.1:n.544C=
ENST00000642041.1:c.*461C= ENSP00000493415.1:n.*461C=
ENST00000369407.3:c.320C= ENSP00000358415.3:p.Thr107=
ENST00000369409.8:c.422C= ENSP00000358417.4:p.Thr141=
ENST00000462324.1:n.690C=
ENST00000493622.5:n.611C=
NM_006623.3:c.422C= NP_006614.2:p.Thr141=
XM_011541226.1:c.644C= XP_011539528.1:p.Thr215=
XM_011541227.1:c.566C= XP_011539529.1:p.Thr189=
XM_011541228.1:c.533C= XP_011539530.1:p.Thr178=
XM_011541229.1:c.359C= XP_011539531.1:p.Thr120=
XM_011541230.1:c.137C= XP_011539532.1:p.Thr46=
XM_011541231.1:c.128C= XP_011539533.1:p.Thr43=
XM_011541226.2:c.644C= XP_011539528.1:p.Thr215=
XM_011541227.2:c.566C= XP_011539529.1:p.Thr189=
XM_011541228.2:c.533C= XP_011539530.1:p.Thr178=
XM_011541231.2:c.128C= XP_011539533.1:p.Thr43=
XM_024446338.1:c.533C= XP_024302106.1:p.Thr178=
NM_006623.4:c.422C= MANE Select NP_006614.2:p.Thr141=