Canonical Allele Identifier: CA1192431830

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727087G= , CM000663.2:g.119727087G=	GRCh38
NC_000001.10:g.120269710G= , CM000663.1:g.120269710G=	GRCh37
NC_000001.9:g.120071233G=	NCBI36
NG_009188.1:g.20292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.495G=	ENSP00000358417.5:p.Gln165=
ENST00000462324.2:n.578G=
ENST00000641023.2:c.495G= MANE Select	ENSP00000493175.1:p.Gln165=
ENST00000641074.1:c.495G=	ENSP00000493446.1:p.Gln165=
ENST00000641115.1:c.495G=	ENSP00000493264.1:p.Gln165=
ENST00000641213.1:c.*148G=	ENSP00000493079.1:n.*148G=
ENST00000641247.1:c.*214G=	ENSP00000492955.1:n.*214G=
ENST00000641272.1:c.429G=	ENSP00000493432.1:p.Gln143=
ENST00000641314.1:n.480G=
ENST00000641371.1:c.409G=	ENSP00000493305.1:p.Val137=
ENST00000641375.1:c.*331G=	ENSP00000493089.1:n.*331G=
ENST00000641455.1:n.40G=
ENST00000641491.1:c.*148G=	ENSP00000493187.1:n.*148G=
ENST00000641570.1:c.*214G=	ENSP00000493213.1:n.*214G=
ENST00000641573.1:n.583G=
ENST00000641587.1:c.*206G=	ENSP00000493453.1:n.*206G=
ENST00000641597.1:c.495G=	ENSP00000493382.1:p.Gln165=
ENST00000641756.1:c.*239G=	ENSP00000493147.1:n.*239G=
ENST00000641811.1:c.251G=
ENST00000641847.1:n.354G=
ENST00000641891.1:c.*321G=	ENSP00000493288.1:n.*321G=
ENST00000641927.1:n.435G=
ENST00000641947.1:c.495G=	ENSP00000492994.1:p.Gln165=
ENST00000642021.1:n.617G=
ENST00000369407.3:c.393G=	ENSP00000358415.3:p.Gln131=
ENST00000369409.8:c.495G=	ENSP00000358417.4:p.Gln165=
ENST00000462324.1:n.763G=
ENST00000493622.5:n.684G=
NM_006623.3:c.495G=	NP_006614.2:p.Gln165=
XM_011541226.1:c.717G=	XP_011539528.1:p.Gln239=
XM_011541227.1:c.639G=	XP_011539529.1:p.Gln213=
XM_011541228.1:c.606G=	XP_011539530.1:p.Gln202=
XM_011541229.1:c.432G=	XP_011539531.1:p.Gln144=
XM_011541230.1:c.210G=	XP_011539532.1:p.Gln70=
XM_011541231.1:c.201G=	XP_011539533.1:p.Gln67=
XM_011541226.2:c.717G=	XP_011539528.1:p.Gln239=
XM_011541227.2:c.639G=	XP_011539529.1:p.Gln213=
XM_011541228.2:c.606G=	XP_011539530.1:p.Gln202=
XM_011541231.2:c.201G=	XP_011539533.1:p.Gln67=
XM_024446338.1:c.606G=	XP_024302106.1:p.Gln202=
NM_006623.4:c.495G= MANE Select	NP_006614.2:p.Gln165=