Canonical Allele Identifier: CA1192434154

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737161C= , CM000663.2:g.119737161C=	GRCh38
NC_000001.10:g.120279784C= , CM000663.1:g.120279784C=	GRCh37
NC_000001.9:g.120081307C=	NCBI36
NG_009188.1:g.30366C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.840C=	ENSP00000358417.5:p.Ser280=
ENST00000641023.2:c.840C= MANE Select	ENSP00000493175.1:p.Ser280=
ENST00000641074.1:c.840C=	ENSP00000493446.1:p.Ser280=
ENST00000641115.1:c.840C=	ENSP00000493264.1:p.Ser280=
ENST00000641213.1:c.*493C=	ENSP00000493079.1:n.*493C=
ENST00000641314.1:n.825C=
ENST00000641375.1:c.*676C=	ENSP00000493089.1:n.*676C=
ENST00000641597.1:c.840C=	ENSP00000493382.1:p.Ser280=
ENST00000641756.1:c.*584C=	ENSP00000493147.1:n.*584C=
ENST00000641811.1:c.596C=
ENST00000641891.1:c.*666C=	ENSP00000493288.1:n.*666C=
ENST00000641927.1:n.780C=
ENST00000641947.1:c.840C=	ENSP00000492994.1:p.Ser280=
ENST00000642021.1:n.962C=
ENST00000369407.3:c.738C=	ENSP00000358415.3:p.Ser246=
ENST00000369409.8:c.840C=	ENSP00000358417.4:p.Ser280=
NM_006623.3:c.840C=	NP_006614.2:p.Ser280=
XM_011541226.1:c.1062C=	XP_011539528.1:p.Ser354=
XM_011541227.1:c.984C=	XP_011539529.1:p.Ser328=
XM_011541228.1:c.951C=	XP_011539530.1:p.Ser317=
XM_011541229.1:c.777C=	XP_011539531.1:p.Ser259=
XM_011541230.1:c.555C=	XP_011539532.1:p.Ser185=
XM_011541231.1:c.546C=	XP_011539533.1:p.Ser182=
XM_011541226.2:c.1062C=	XP_011539528.1:p.Ser354=
XM_011541227.2:c.984C=	XP_011539529.1:p.Ser328=
XM_011541228.2:c.951C=	XP_011539530.1:p.Ser317=
XM_011541231.2:c.546C=	XP_011539533.1:p.Ser182=
XM_024446338.1:c.951C=	XP_024302106.1:p.Ser317=
NM_006623.4:c.840C= MANE Select	NP_006614.2:p.Ser280=