Canonical Allele Identifier: CA1143538241

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119735432G= , CM000663.2:g.119735432G=	GRCh38
NC_000001.10:g.120278055G= , CM000663.1:g.120278055G=	GRCh37
NC_000001.9:g.120079578G=	NCBI36
NG_009188.1:g.28637G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.781G=	ENSP00000358417.5:p.Val261=
ENST00000469443.2:n.601G=
ENST00000641023.2:c.781G= MANE Select	ENSP00000493175.1:p.Val261=
ENST00000641074.1:c.781G=	ENSP00000493446.1:p.Val261=
ENST00000641115.1:c.781G=	ENSP00000493264.1:p.Val261=
ENST00000641213.1:c.*434G=	ENSP00000493079.1:n.*434G=
ENST00000641272.1:c.715G=	ENSP00000493432.1:p.Val239=
ENST00000641314.1:n.766G=
ENST00000641375.1:c.*617G=	ENSP00000493089.1:n.*617G=
ENST00000641597.1:c.781G=	ENSP00000493382.1:p.Val261=
ENST00000641756.1:c.*525G=	ENSP00000493147.1:n.*525G=
ENST00000641811.1:c.537G=
ENST00000641891.1:c.*607G=	ENSP00000493288.1:n.*607G=
ENST00000641927.1:n.721G=
ENST00000641947.1:c.781G=	ENSP00000492994.1:p.Val261=
ENST00000642021.1:n.903G=
ENST00000369407.3:c.679G=	ENSP00000358415.3:p.Val227=
ENST00000369409.8:c.781G=	ENSP00000358417.4:p.Val261=
NM_006623.3:c.781G=	NP_006614.2:p.Val261=
XM_011541226.1:c.1003G=	XP_011539528.1:p.Val335=
XM_011541227.1:c.925G=	XP_011539529.1:p.Val309=
XM_011541228.1:c.892G=	XP_011539530.1:p.Val298=
XM_011541229.1:c.718G=	XP_011539531.1:p.Val240=
XM_011541230.1:c.496G=	XP_011539532.1:p.Val166=
XM_011541231.1:c.487G=	XP_011539533.1:p.Val163=
XM_011541226.2:c.1003G=	XP_011539528.1:p.Val335=
XM_011541227.2:c.925G=	XP_011539529.1:p.Val309=
XM_011541228.2:c.892G=	XP_011539530.1:p.Val298=
XM_011541231.2:c.487G=	XP_011539533.1:p.Val163=
XM_024446338.1:c.892G=	XP_024302106.1:p.Val298=
NM_006623.4:c.781G= MANE Select	NP_006614.2:p.Val261=