Canonical Allele Identifier: CA1142314692

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727088T= , CM000663.2:g.119727088T=	GRCh38
NC_000001.10:g.120269711T= , CM000663.1:g.120269711T=	GRCh37
NC_000001.9:g.120071234T=	NCBI36
NG_009188.1:g.20293T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.496T=	ENSP00000358417.5:p.Ser166=
ENST00000462324.2:n.579T=
ENST00000641023.2:c.496T= MANE Select	ENSP00000493175.1:p.Ser166=
ENST00000641074.1:c.496T=	ENSP00000493446.1:p.Ser166=
ENST00000641115.1:c.496T=	ENSP00000493264.1:p.Ser166=
ENST00000641213.1:c.*149T=	ENSP00000493079.1:n.*149T=
ENST00000641247.1:c.*215T=	ENSP00000492955.1:n.*215T=
ENST00000641272.1:c.430T=	ENSP00000493432.1:p.Ser144=
ENST00000641314.1:n.481T=
ENST00000641371.1:c.410T=	ENSP00000493305.1:p.Val137=
ENST00000641375.1:c.*332T=	ENSP00000493089.1:n.*332T=
ENST00000641455.1:n.41T=
ENST00000641491.1:c.*149T=	ENSP00000493187.1:n.*149T=
ENST00000641570.1:c.*215T=	ENSP00000493213.1:n.*215T=
ENST00000641573.1:n.584T=
ENST00000641587.1:c.*207T=	ENSP00000493453.1:n.*207T=
ENST00000641597.1:c.496T=	ENSP00000493382.1:p.Ser166=
ENST00000641756.1:c.*240T=	ENSP00000493147.1:n.*240T=
ENST00000641811.1:c.252T=
ENST00000641847.1:n.355T=
ENST00000641891.1:c.*322T=	ENSP00000493288.1:n.*322T=
ENST00000641927.1:n.436T=
ENST00000641947.1:c.496T=	ENSP00000492994.1:p.Ser166=
ENST00000642021.1:n.618T=
ENST00000369407.3:c.394T=	ENSP00000358415.3:p.Ser132=
ENST00000369409.8:c.496T=	ENSP00000358417.4:p.Ser166=
ENST00000462324.1:n.764T=
ENST00000493622.5:n.685T=
NM_006623.3:c.496T=	NP_006614.2:p.Ser166=
XM_011541226.1:c.718T=	XP_011539528.1:p.Ser240=
XM_011541227.1:c.640T=	XP_011539529.1:p.Ser214=
XM_011541228.1:c.607T=	XP_011539530.1:p.Ser203=
XM_011541229.1:c.433T=	XP_011539531.1:p.Ser145=
XM_011541230.1:c.211T=	XP_011539532.1:p.Ser71=
XM_011541231.1:c.202T=	XP_011539533.1:p.Ser68=
XM_011541226.2:c.718T=	XP_011539528.1:p.Ser240=
XM_011541227.2:c.640T=	XP_011539529.1:p.Ser214=
XM_011541228.2:c.607T=	XP_011539530.1:p.Ser203=
XM_011541231.2:c.202T=	XP_011539533.1:p.Ser68=
XM_024446338.1:c.607T=	XP_024302106.1:p.Ser203=
NM_006623.4:c.496T= MANE Select	NP_006614.2:p.Ser166=