Canonical Allele Identifier: CA1192434167

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737175G= , CM000663.2:g.119737175G=	GRCh38
NC_000001.10:g.120279798G= , CM000663.1:g.120279798G=	GRCh37
NC_000001.9:g.120081321G=	NCBI36
NG_009188.1:g.30380G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.854G=	ENSP00000358417.5:p.Gly285=
ENST00000641023.2:c.854G= MANE Select	ENSP00000493175.1:p.Gly285=
ENST00000641074.1:c.854G=	ENSP00000493446.1:p.Gly285=
ENST00000641115.1:c.854G=	ENSP00000493264.1:p.Gly285=
ENST00000641213.1:c.*507G=	ENSP00000493079.1:n.*507G=
ENST00000641314.1:n.839G=
ENST00000641375.1:c.*690G=	ENSP00000493089.1:n.*690G=
ENST00000641597.1:c.854G=	ENSP00000493382.1:p.Gly285=
ENST00000641756.1:c.*598G=	ENSP00000493147.1:n.*598G=
ENST00000641811.1:c.610G=
ENST00000641891.1:c.*680G=	ENSP00000493288.1:n.*680G=
ENST00000641927.1:n.794G=
ENST00000641947.1:c.854G=	ENSP00000492994.1:p.Gly285=
ENST00000642021.1:n.976G=
ENST00000369407.3:c.752G=	ENSP00000358415.3:p.Gly251=
ENST00000369409.8:c.854G=	ENSP00000358417.4:p.Gly285=
NM_006623.3:c.854G=	NP_006614.2:p.Gly285=
XM_011541226.1:c.1076G=	XP_011539528.1:p.Gly359=
XM_011541227.1:c.998G=	XP_011539529.1:p.Gly333=
XM_011541228.1:c.965G=	XP_011539530.1:p.Gly322=
XM_011541229.1:c.791G=	XP_011539531.1:p.Gly264=
XM_011541230.1:c.569G=	XP_011539532.1:p.Gly190=
XM_011541231.1:c.560G=	XP_011539533.1:p.Gly187=
XM_011541226.2:c.1076G=	XP_011539528.1:p.Gly359=
XM_011541227.2:c.998G=	XP_011539529.1:p.Gly333=
XM_011541228.2:c.965G=	XP_011539530.1:p.Gly322=
XM_011541231.2:c.560G=	XP_011539533.1:p.Gly187=
XM_024446338.1:c.965G=	XP_024302106.1:p.Gly322=
NM_006623.4:c.854G= MANE Select	NP_006614.2:p.Gly285=