Canonical Allele Identifier: CA1148224509

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737114G= , CM000663.2:g.119737114G=	GRCh38
NC_000001.10:g.120279737G= , CM000663.1:g.120279737G=	GRCh37
NC_000001.9:g.120081260G=	NCBI36
NG_009188.1:g.30319G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.793G=	ENSP00000358417.5:p.Glu265=
ENST00000469443.2:n.613G=
ENST00000641023.2:c.793G= MANE Select	ENSP00000493175.1:p.Glu265=
ENST00000641074.1:c.793G=	ENSP00000493446.1:p.Glu265=
ENST00000641115.1:c.793G=	ENSP00000493264.1:p.Glu265=
ENST00000641213.1:c.*446G=	ENSP00000493079.1:n.*446G=
ENST00000641314.1:n.778G=
ENST00000641375.1:c.*629G=	ENSP00000493089.1:n.*629G=
ENST00000641597.1:c.793G=	ENSP00000493382.1:p.Glu265=
ENST00000641756.1:c.*537G=	ENSP00000493147.1:n.*537G=
ENST00000641811.1:c.549G=
ENST00000641891.1:c.*619G=	ENSP00000493288.1:n.*619G=
ENST00000641927.1:n.733G=
ENST00000641947.1:c.793G=	ENSP00000492994.1:p.Glu265=
ENST00000642021.1:n.915G=
ENST00000369407.3:c.691G=	ENSP00000358415.3:p.Glu231=
ENST00000369409.8:c.793G=	ENSP00000358417.4:p.Glu265=
NM_006623.3:c.793G=	NP_006614.2:p.Glu265=
XM_011541226.1:c.1015G=	XP_011539528.1:p.Glu339=
XM_011541227.1:c.937G=	XP_011539529.1:p.Glu313=
XM_011541228.1:c.904G=	XP_011539530.1:p.Glu302=
XM_011541229.1:c.730G=	XP_011539531.1:p.Glu244=
XM_011541230.1:c.508G=	XP_011539532.1:p.Glu170=
XM_011541231.1:c.499G=	XP_011539533.1:p.Glu167=
XM_011541226.2:c.1015G=	XP_011539528.1:p.Glu339=
XM_011541227.2:c.937G=	XP_011539529.1:p.Glu313=
XM_011541228.2:c.904G=	XP_011539530.1:p.Glu302=
XM_011541231.2:c.499G=	XP_011539533.1:p.Glu167=
XM_024446338.1:c.904G=	XP_024302106.1:p.Glu302=
NM_006623.4:c.793G= MANE Select	NP_006614.2:p.Glu265=