Canonical Allele Identifier: CA1192431737

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119726868C= , CM000663.2:g.119726868C=	GRCh38
NC_000001.10:g.120269491C= , CM000663.1:g.120269491C=	GRCh37
NC_000001.9:g.120071014C=	NCBI36
NG_009188.1:g.20073C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.374C=	ENSP00000358417.5:p.Thr125=
ENST00000462324.2:n.457C=
ENST00000641023.2:c.374C= MANE Select	ENSP00000493175.1:p.Thr125=
ENST00000641074.1:c.374C=	ENSP00000493446.1:p.Thr125=
ENST00000641115.1:c.374C=	ENSP00000493264.1:p.Thr125=
ENST00000641213.1:c.*27C=	ENSP00000493079.1:n.*27C=
ENST00000641247.1:c.*93C=	ENSP00000492955.1:n.*93C=
ENST00000641272.1:c.308C=	ENSP00000493432.1:p.Thr103=
ENST00000641314.1:n.359C=
ENST00000641371.1:c.288C=	ENSP00000493305.1:p.Asp96=
ENST00000641375.1:c.*210C=	ENSP00000493089.1:n.*210C=
ENST00000641491.1:c.*27C=	ENSP00000493187.1:n.*27C=
ENST00000641513.1:c.*118C=	ENSP00000493398.1:n.*118C=
ENST00000641570.1:c.*93C=	ENSP00000493213.1:n.*93C=
ENST00000641573.1:n.462C=
ENST00000641587.1:c.*85C=	ENSP00000493453.1:n.*85C=
ENST00000641597.1:c.374C=	ENSP00000493382.1:p.Thr125=
ENST00000641711.1:n.598C=
ENST00000641756.1:c.*118C=	ENSP00000493147.1:n.*118C=
ENST00000641811.1:c.130C=
ENST00000641847.1:n.233C=
ENST00000641891.1:c.*200C=	ENSP00000493288.1:n.*200C=
ENST00000641927.1:n.314C=
ENST00000641947.1:c.374C=	ENSP00000492994.1:p.Thr125=
ENST00000642021.1:n.496C=
ENST00000642041.1:c.*413C=	ENSP00000493415.1:n.*413C=
ENST00000369407.3:c.272C=	ENSP00000358415.3:p.Thr91=
ENST00000369409.8:c.374C=	ENSP00000358417.4:p.Thr125=
ENST00000462324.1:n.642C=
ENST00000493622.5:n.563C=
NM_006623.3:c.374C=	NP_006614.2:p.Thr125=
XM_011541226.1:c.596C=	XP_011539528.1:p.Thr199=
XM_011541227.1:c.518C=	XP_011539529.1:p.Thr173=
XM_011541228.1:c.485C=	XP_011539530.1:p.Thr162=
XM_011541229.1:c.311C=	XP_011539531.1:p.Thr104=
XM_011541230.1:c.89C=	XP_011539532.1:p.Thr30=
XM_011541231.1:c.80C=	XP_011539533.1:p.Thr27=
XM_011541226.2:c.596C=	XP_011539528.1:p.Thr199=
XM_011541227.2:c.518C=	XP_011539529.1:p.Thr173=
XM_011541228.2:c.485C=	XP_011539530.1:p.Thr162=
XM_011541231.2:c.80C=	XP_011539533.1:p.Thr27=
XM_024446338.1:c.485C=	XP_024302106.1:p.Thr162=
NM_006623.4:c.374C= MANE Select	NP_006614.2:p.Thr125=