Canonical Allele Identifier: CA341847673

Gene: PHGDH

Linked Data

• MyVariant Identifiers: chr1:g.120269633G>C (hg19) ; chr1:g.119727010G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727010G>C , CM000663.2:g.119727010G>C	GRCh38
NC_000001.10:g.120269633G>C , CM000663.1:g.120269633G>C	GRCh37
NC_000001.9:g.120071156G>C	NCBI36
NG_009188.1:g.20215G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.418G>C	ENSP00000358417.5:p.Gly140Arg
ENST00000462324.2:n.501G>C
ENST00000641023.2:c.418G>C MANE Select	ENSP00000493175.1:p.Gly140Arg
ENST00000641074.1:c.418G>C	ENSP00000493446.1:p.Gly140Arg
ENST00000641115.1:c.418G>C	ENSP00000493264.1:p.Gly140Arg
ENST00000641213.1:c.*71G>C	ENSP00000493079.1:n.*71G>C
ENST00000641247.1:c.*137G>C	ENSP00000492955.1:n.*137G>C
ENST00000641272.1:c.352G>C	ENSP00000493432.1:p.Gly118Arg
ENST00000641314.1:n.403G>C
ENST00000641371.1:c.332G>C	ENSP00000493305.1:p.Gly111Ala
ENST00000641375.1:c.*254G>C	ENSP00000493089.1:n.*254G>C
ENST00000641491.1:c.*71G>C	ENSP00000493187.1:n.*71G>C
ENST00000641570.1:c.*137G>C	ENSP00000493213.1:n.*137G>C
ENST00000641573.1:n.506G>C
ENST00000641587.1:c.*129G>C	ENSP00000493453.1:n.*129G>C
ENST00000641597.1:c.418G>C	ENSP00000493382.1:p.Gly140Arg
ENST00000641711.1:n.642G>C
ENST00000641756.1:c.*162G>C	ENSP00000493147.1:n.*162G>C
ENST00000641811.1:c.174G>C
ENST00000641847.1:n.277G>C
ENST00000641891.1:c.*244G>C	ENSP00000493288.1:n.*244G>C
ENST00000641927.1:n.358G>C
ENST00000641947.1:c.418G>C	ENSP00000492994.1:p.Gly140Arg
ENST00000642021.1:n.540G>C
ENST00000642041.1:c.*457G>C	ENSP00000493415.1:n.*457G>C
ENST00000369407.3:c.316G>C	ENSP00000358415.3:p.Gly106Arg
ENST00000369409.8:c.418G>C	ENSP00000358417.4:p.Gly140Arg
ENST00000462324.1:n.686G>C
ENST00000493622.5:n.607G>C
NM_006623.3:c.418G>C	NP_006614.2:p.Gly140Arg
XM_011541226.1:c.640G>C	XP_011539528.1:p.Gly214Arg
XM_011541227.1:c.562G>C	XP_011539529.1:p.Gly188Arg
XM_011541228.1:c.529G>C	XP_011539530.1:p.Gly177Arg
XM_011541229.1:c.355G>C	XP_011539531.1:p.Gly119Arg
XM_011541230.1:c.133G>C	XP_011539532.1:p.Gly45Arg
XM_011541231.1:c.124G>C	XP_011539533.1:p.Gly42Arg
XM_011541226.2:c.640G>C	XP_011539528.1:p.Gly214Arg
XM_011541227.2:c.562G>C	XP_011539529.1:p.Gly188Arg
XM_011541228.2:c.529G>C	XP_011539530.1:p.Gly177Arg
XM_011541231.2:c.124G>C	XP_011539533.1:p.Gly42Arg
XM_024446338.1:c.529G>C	XP_024302106.1:p.Gly177Arg
NM_006623.4:c.418G>C MANE Select	NP_006614.2:p.Gly140Arg