Canonical Allele Identifier: CA1192431741

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119726883A= , CM000663.2:g.119726883A=	GRCh38
NC_000001.10:g.120269506A= , CM000663.1:g.120269506A=	GRCh37
NC_000001.9:g.120071029A=	NCBI36
NG_009188.1:g.20088A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.389A=	ENSP00000358417.5:p.Asp130=
ENST00000462324.2:n.472A=
ENST00000641023.2:c.389A= MANE Select	ENSP00000493175.1:p.Asp130=
ENST00000641074.1:c.389A=	ENSP00000493446.1:p.Asp130=
ENST00000641115.1:c.389A=	ENSP00000493264.1:p.Asp130=
ENST00000641213.1:c.*42A=	ENSP00000493079.1:n.*42A=
ENST00000641247.1:c.*108A=	ENSP00000492955.1:n.*108A=
ENST00000641272.1:c.323A=	ENSP00000493432.1:p.Asp108=
ENST00000641314.1:n.374A=
ENST00000641371.1:c.303A=	ENSP00000493305.1:p.Gly101=
ENST00000641375.1:c.*225A=	ENSP00000493089.1:n.*225A=
ENST00000641491.1:c.*42A=	ENSP00000493187.1:n.*42A=
ENST00000641513.1:c.*133A=	ENSP00000493398.1:n.*133A=
ENST00000641570.1:c.*108A=	ENSP00000493213.1:n.*108A=
ENST00000641573.1:n.477A=
ENST00000641587.1:c.*100A=	ENSP00000493453.1:n.*100A=
ENST00000641597.1:c.389A=	ENSP00000493382.1:p.Asp130=
ENST00000641711.1:n.613A=
ENST00000641756.1:c.*133A=	ENSP00000493147.1:n.*133A=
ENST00000641811.1:c.145A=
ENST00000641847.1:n.248A=
ENST00000641891.1:c.*215A=	ENSP00000493288.1:n.*215A=
ENST00000641927.1:n.329A=
ENST00000641947.1:c.389A=	ENSP00000492994.1:p.Asp130=
ENST00000642021.1:n.511A=
ENST00000642041.1:c.*428A=	ENSP00000493415.1:n.*428A=
ENST00000369407.3:c.287A=	ENSP00000358415.3:p.Asp96=
ENST00000369409.8:c.389A=	ENSP00000358417.4:p.Asp130=
ENST00000462324.1:n.657A=
ENST00000493622.5:n.578A=
NM_006623.3:c.389A=	NP_006614.2:p.Asp130=
XM_011541226.1:c.611A=	XP_011539528.1:p.Asp204=
XM_011541227.1:c.533A=	XP_011539529.1:p.Asp178=
XM_011541228.1:c.500A=	XP_011539530.1:p.Asp167=
XM_011541229.1:c.326A=	XP_011539531.1:p.Asp109=
XM_011541230.1:c.104A=	XP_011539532.1:p.Asp35=
XM_011541231.1:c.95A=	XP_011539533.1:p.Asp32=
XM_011541226.2:c.611A=	XP_011539528.1:p.Asp204=
XM_011541227.2:c.533A=	XP_011539529.1:p.Asp178=
XM_011541228.2:c.500A=	XP_011539530.1:p.Asp167=
XM_011541231.2:c.95A=	XP_011539533.1:p.Asp32=
XM_024446338.1:c.500A=	XP_024302106.1:p.Asp167=
NM_006623.4:c.389A= MANE Select	NP_006614.2:p.Asp130=