Canonical Allele Identifier: CA1142204483

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737155C= , CM000663.2:g.119737155C=	GRCh38
NC_000001.10:g.120279778C= , CM000663.1:g.120279778C=	GRCh37
NC_000001.9:g.120081301C=	NCBI36
NG_009188.1:g.30360C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.834C=	ENSP00000358417.5:p.Val278=
ENST00000641023.2:c.834C= MANE Select	ENSP00000493175.1:p.Val278=
ENST00000641074.1:c.834C=	ENSP00000493446.1:p.Val278=
ENST00000641115.1:c.834C=	ENSP00000493264.1:p.Val278=
ENST00000641213.1:c.*487C=	ENSP00000493079.1:n.*487C=
ENST00000641314.1:n.819C=
ENST00000641375.1:c.*670C=	ENSP00000493089.1:n.*670C=
ENST00000641597.1:c.834C=	ENSP00000493382.1:p.Val278=
ENST00000641756.1:c.*578C=	ENSP00000493147.1:n.*578C=
ENST00000641811.1:c.590C=
ENST00000641891.1:c.*660C=	ENSP00000493288.1:n.*660C=
ENST00000641927.1:n.774C=
ENST00000641947.1:c.834C=	ENSP00000492994.1:p.Val278=
ENST00000642021.1:n.956C=
ENST00000369407.3:c.732C=	ENSP00000358415.3:p.Val244=
ENST00000369409.8:c.834C=	ENSP00000358417.4:p.Val278=
NM_006623.3:c.834C=	NP_006614.2:p.Val278=
XM_011541226.1:c.1056C=	XP_011539528.1:p.Val352=
XM_011541227.1:c.978C=	XP_011539529.1:p.Val326=
XM_011541228.1:c.945C=	XP_011539530.1:p.Val315=
XM_011541229.1:c.771C=	XP_011539531.1:p.Val257=
XM_011541230.1:c.549C=	XP_011539532.1:p.Val183=
XM_011541231.1:c.540C=	XP_011539533.1:p.Val180=
XM_011541226.2:c.1056C=	XP_011539528.1:p.Val352=
XM_011541227.2:c.978C=	XP_011539529.1:p.Val326=
XM_011541228.2:c.945C=	XP_011539530.1:p.Val315=
XM_011541231.2:c.540C=	XP_011539533.1:p.Val180=
XM_024446338.1:c.945C=	XP_024302106.1:p.Val315=
NM_006623.4:c.834C= MANE Select	NP_006614.2:p.Val278=