Canonical Allele Identifier: CA1148224514

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727010G= , CM000663.2:g.119727010G=	GRCh38
NC_000001.10:g.120269633G= , CM000663.1:g.120269633G=	GRCh37
NC_000001.9:g.120071156G=	NCBI36
NG_009188.1:g.20215G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.418G=	ENSP00000358417.5:p.Gly140=
ENST00000462324.2:n.501G=
ENST00000641023.2:c.418G= MANE Select	ENSP00000493175.1:p.Gly140=
ENST00000641074.1:c.418G=	ENSP00000493446.1:p.Gly140=
ENST00000641115.1:c.418G=	ENSP00000493264.1:p.Gly140=
ENST00000641213.1:c.*71G=	ENSP00000493079.1:n.*71G=
ENST00000641247.1:c.*137G=	ENSP00000492955.1:n.*137G=
ENST00000641272.1:c.352G=	ENSP00000493432.1:p.Gly118=
ENST00000641314.1:n.403G=
ENST00000641371.1:c.332G=	ENSP00000493305.1:p.Gly111=
ENST00000641375.1:c.*254G=	ENSP00000493089.1:n.*254G=
ENST00000641491.1:c.*71G=	ENSP00000493187.1:n.*71G=
ENST00000641570.1:c.*137G=	ENSP00000493213.1:n.*137G=
ENST00000641573.1:n.506G=
ENST00000641587.1:c.*129G=	ENSP00000493453.1:n.*129G=
ENST00000641597.1:c.418G=	ENSP00000493382.1:p.Gly140=
ENST00000641711.1:n.642G=
ENST00000641756.1:c.*162G=	ENSP00000493147.1:n.*162G=
ENST00000641811.1:c.174G=
ENST00000641847.1:n.277G=
ENST00000641891.1:c.*244G=	ENSP00000493288.1:n.*244G=
ENST00000641927.1:n.358G=
ENST00000641947.1:c.418G=	ENSP00000492994.1:p.Gly140=
ENST00000642021.1:n.540G=
ENST00000642041.1:c.*457G=	ENSP00000493415.1:n.*457G=
ENST00000369407.3:c.316G=	ENSP00000358415.3:p.Gly106=
ENST00000369409.8:c.418G=	ENSP00000358417.4:p.Gly140=
ENST00000462324.1:n.686G=
ENST00000493622.5:n.607G=
NM_006623.3:c.418G=	NP_006614.2:p.Gly140=
XM_011541226.1:c.640G=	XP_011539528.1:p.Gly214=
XM_011541227.1:c.562G=	XP_011539529.1:p.Gly188=
XM_011541228.1:c.529G=	XP_011539530.1:p.Gly177=
XM_011541229.1:c.355G=	XP_011539531.1:p.Gly119=
XM_011541230.1:c.133G=	XP_011539532.1:p.Gly45=
XM_011541231.1:c.124G=	XP_011539533.1:p.Gly42=
XM_011541226.2:c.640G=	XP_011539528.1:p.Gly214=
XM_011541227.2:c.562G=	XP_011539529.1:p.Gly188=
XM_011541228.2:c.529G=	XP_011539530.1:p.Gly177=
XM_011541231.2:c.124G=	XP_011539533.1:p.Gly42=
XM_024446338.1:c.529G=	XP_024302106.1:p.Gly177=
NM_006623.4:c.418G= MANE Select	NP_006614.2:p.Gly140=