Canonical Allele Identifier: CA1148722865

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119726947C= , CM000663.2:g.119726947C=	GRCh38
NC_000001.10:g.120269570C= , CM000663.1:g.120269570C=	GRCh37
NC_000001.9:g.120071093C=	NCBI36
NG_009188.1:g.20152C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.411+42C=	ENSP00000358417.5:n.411+42C=
ENST00000462324.2:n.494+42C=
ENST00000641023.2:c.411+42C= MANE Select	ENSP00000493175.1:n.411+42C=
ENST00000641074.1:c.411+42C=	ENSP00000493446.1:n.411+42C=
ENST00000641115.1:c.411+42C=	ENSP00000493264.1:n.411+42C=
ENST00000641213.1:c.*64+42C=	ENSP00000493079.1:n.*64+42C=
ENST00000641247.1:c.*130+42C=	ENSP00000492955.1:n.*130+42C=
ENST00000641272.1:c.345+42C=	ENSP00000493432.1:n.345+42C=
ENST00000641314.1:n.396+42C=
ENST00000641371.1:c.325+42C=	ENSP00000493305.1:n.325+42C=
ENST00000641375.1:c.*247+42C=	ENSP00000493089.1:n.*247+42C=
ENST00000641491.1:c.*64+42C=	ENSP00000493187.1:n.*64+42C=
ENST00000641570.1:c.*130+42C=	ENSP00000493213.1:n.*130+42C=
ENST00000641573.1:n.499+42C=
ENST00000641587.1:c.*122+42C=	ENSP00000493453.1:n.*122+42C=
ENST00000641597.1:c.411+42C=	ENSP00000493382.1:n.411+42C=
ENST00000641711.1:n.635+42C=
ENST00000641756.1:c.*155+42C=	ENSP00000493147.1:n.*155+42C=
ENST00000641811.1:c.167+42C=
ENST00000641847.1:n.270+42C=
ENST00000641891.1:c.*237+42C=	ENSP00000493288.1:n.*237+42C=
ENST00000641927.1:n.351+42C=
ENST00000641947.1:c.411+42C=	ENSP00000492994.1:n.411+42C=
ENST00000642021.1:n.533+42C=
ENST00000642041.1:c.*450+42C=	ENSP00000493415.1:n.*450+42C=
ENST00000369407.3:c.309+42C=	ENSP00000358415.3:n.309+42C=
ENST00000369409.8:c.411+42C=	ENSP00000358417.4:n.411+42C=
ENST00000462324.1:n.679+42C=
ENST00000493622.5:n.600+42C=
NM_006623.3:c.411+42C=	NP_006614.2:n.411+42C=
XM_011541226.1:c.633+42C=	XP_011539528.1:n.633+42C=
XM_011541227.1:c.555+42C=	XP_011539529.1:n.555+42C=
XM_011541228.1:c.522+42C=	XP_011539530.1:n.522+42C=
XM_011541229.1:c.348+42C=	XP_011539531.1:n.348+42C=
XM_011541230.1:c.126+42C=	XP_011539532.1:n.126+42C=
XM_011541231.1:c.117+42C=	XP_011539533.1:n.117+42C=
XM_011541226.2:c.633+42C=	XP_011539528.1:n.633+42C=
XM_011541227.2:c.555+42C=	XP_011539529.1:n.555+42C=
XM_011541228.2:c.522+42C=	XP_011539530.1:n.522+42C=
XM_011541231.2:c.117+42C=	XP_011539533.1:n.117+42C=
XM_024446338.1:c.522+42C=	XP_024302106.1:n.522+42C=
NM_006623.4:c.411+42C= MANE Select	NP_006614.2:n.411+42C=