Canonical Allele Identifier: CA1141581011

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119742870G= , CM000663.2:g.119742870G=	GRCh38
NC_000001.10:g.120285493G= , CM000663.1:g.120285493G=	GRCh37
NC_000001.9:g.120087016G=	NCBI36
NG_009188.1:g.36075G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.1273G=	ENSP00000358417.5:p.Val425=
ENST00000641023.2:c.1273G= MANE Select	ENSP00000493175.1:p.Val425=
ENST00000641074.1:c.1142G=	ENSP00000493446.1:p.Arg381=
ENST00000641115.1:c.1009G=	ENSP00000493264.1:p.Val337=
ENST00000641213.1:c.*926G=	ENSP00000493079.1:n.*926G=
ENST00000641314.1:n.1258G=
ENST00000641375.1:c.*1109G=	ENSP00000493089.1:n.*1109G=
ENST00000641597.1:c.1273G=	ENSP00000493382.1:p.Val425=
ENST00000641756.1:c.*1017G=	ENSP00000493147.1:n.*1017G=
ENST00000641811.1:c.702-1016G=
ENST00000641891.1:c.*1099G=	ENSP00000493288.1:n.*1099G=
ENST00000641927.1:n.1213G=
ENST00000641939.1:n.398G=
ENST00000641947.1:c.1252G=	ENSP00000492994.1:p.Val418=
ENST00000642021.1:n.2304G=
ENST00000369407.3:c.1171G=	ENSP00000358415.3:p.Val391=
ENST00000369409.8:c.1273G=	ENSP00000358417.4:p.Val425=
ENST00000482968.1:n.1252G=
NM_006623.3:c.1273G=	NP_006614.2:p.Val425=
XM_011541226.1:c.1495G=	XP_011539528.1:p.Val499=
XM_011541227.1:c.1417G=	XP_011539529.1:p.Val473=
XM_011541228.1:c.1384G=	XP_011539530.1:p.Val462=
XM_011541229.1:c.1210G=	XP_011539531.1:p.Val404=
XM_011541230.1:c.988G=	XP_011539532.1:p.Val330=
XM_011541231.1:c.979G=	XP_011539533.1:p.Val327=
XM_011541226.2:c.1495G=	XP_011539528.1:p.Val499=
XM_011541227.2:c.1417G=	XP_011539529.1:p.Val473=
XM_011541228.2:c.1384G=	XP_011539530.1:p.Val462=
XM_011541231.2:c.979G=	XP_011539533.1:p.Val327=
XM_024446338.1:c.1384G=	XP_024302106.1:p.Val462=
NM_006623.4:c.1273G= MANE Select	NP_006614.2:p.Val425=