Canonical Allele Identifier: CA1192434139

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737129C= , CM000663.2:g.119737129C=	GRCh38
NC_000001.10:g.120279752C= , CM000663.1:g.120279752C=	GRCh37
NC_000001.9:g.120081275C=	NCBI36
NG_009188.1:g.30334C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.808C=	ENSP00000358417.5:p.Arg270=
ENST00000469443.2:n.628C=
ENST00000641023.2:c.808C= MANE Select	ENSP00000493175.1:p.Arg270=
ENST00000641074.1:c.808C=	ENSP00000493446.1:p.Arg270=
ENST00000641115.1:c.808C=	ENSP00000493264.1:p.Arg270=
ENST00000641213.1:c.*461C=	ENSP00000493079.1:n.*461C=
ENST00000641314.1:n.793C=
ENST00000641375.1:c.*644C=	ENSP00000493089.1:n.*644C=
ENST00000641597.1:c.808C=	ENSP00000493382.1:p.Arg270=
ENST00000641756.1:c.*552C=	ENSP00000493147.1:n.*552C=
ENST00000641811.1:c.564C=
ENST00000641891.1:c.*634C=	ENSP00000493288.1:n.*634C=
ENST00000641927.1:n.748C=
ENST00000641947.1:c.808C=	ENSP00000492994.1:p.Arg270=
ENST00000642021.1:n.930C=
ENST00000369407.3:c.706C=	ENSP00000358415.3:p.Arg236=
ENST00000369409.8:c.808C=	ENSP00000358417.4:p.Arg270=
NM_006623.3:c.808C=	NP_006614.2:p.Arg270=
XM_011541226.1:c.1030C=	XP_011539528.1:p.Arg344=
XM_011541227.1:c.952C=	XP_011539529.1:p.Arg318=
XM_011541228.1:c.919C=	XP_011539530.1:p.Arg307=
XM_011541229.1:c.745C=	XP_011539531.1:p.Arg249=
XM_011541230.1:c.523C=	XP_011539532.1:p.Arg175=
XM_011541231.1:c.514C=	XP_011539533.1:p.Arg172=
XM_011541226.2:c.1030C=	XP_011539528.1:p.Arg344=
XM_011541227.2:c.952C=	XP_011539529.1:p.Arg318=
XM_011541228.2:c.919C=	XP_011539530.1:p.Arg307=
XM_011541231.2:c.514C=	XP_011539533.1:p.Arg172=
XM_024446338.1:c.919C=	XP_024302106.1:p.Arg307=
NM_006623.4:c.808C= MANE Select	NP_006614.2:p.Arg270=