Canonical Allele Identifier: CA1192431730

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119726854G= , CM000663.2:g.119726854G=	GRCh38
NC_000001.10:g.120269477G= , CM000663.1:g.120269477G=	GRCh37
NC_000001.9:g.120071000G=	NCBI36
NG_009188.1:g.20059G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.360G=	ENSP00000358417.5:p.Gln120=
ENST00000462324.2:n.443G=
ENST00000641023.2:c.360G= MANE Select	ENSP00000493175.1:p.Gln120=
ENST00000641074.1:c.360G=	ENSP00000493446.1:p.Gln120=
ENST00000641115.1:c.360G=	ENSP00000493264.1:p.Gln120=
ENST00000641213.1:c.*13G=	ENSP00000493079.1:n.*13G=
ENST00000641247.1:c.*79G=	ENSP00000492955.1:n.*79G=
ENST00000641272.1:c.294G=	ENSP00000493432.1:p.Gln98=
ENST00000641314.1:n.345G=
ENST00000641371.1:c.274G=	ENSP00000493305.1:p.Asp92=
ENST00000641375.1:c.*196G=	ENSP00000493089.1:n.*196G=
ENST00000641491.1:c.*13G=	ENSP00000493187.1:n.*13G=
ENST00000641513.1:c.*104G=	ENSP00000493398.1:n.*104G=
ENST00000641570.1:c.*79G=	ENSP00000493213.1:n.*79G=
ENST00000641573.1:n.448G=
ENST00000641587.1:c.*71G=	ENSP00000493453.1:n.*71G=
ENST00000641597.1:c.360G=	ENSP00000493382.1:p.Gln120=
ENST00000641711.1:n.584G=
ENST00000641756.1:c.*104G=	ENSP00000493147.1:n.*104G=
ENST00000641811.1:c.116G=
ENST00000641847.1:n.219G=
ENST00000641891.1:c.*186G=	ENSP00000493288.1:n.*186G=
ENST00000641927.1:n.300G=
ENST00000641947.1:c.360G=	ENSP00000492994.1:p.Gln120=
ENST00000642021.1:n.482G=
ENST00000642041.1:c.*399G=	ENSP00000493415.1:n.*399G=
ENST00000369407.3:c.258G=	ENSP00000358415.3:p.Gln86=
ENST00000369409.8:c.360G=	ENSP00000358417.4:p.Gln120=
ENST00000462324.1:n.628G=
ENST00000493622.5:n.549G=
NM_006623.3:c.360G=	NP_006614.2:p.Gln120=
XM_011541226.1:c.582G=	XP_011539528.1:p.Gln194=
XM_011541227.1:c.504G=	XP_011539529.1:p.Gln168=
XM_011541228.1:c.471G=	XP_011539530.1:p.Gln157=
XM_011541229.1:c.297G=	XP_011539531.1:p.Gln99=
XM_011541230.1:c.75G=	XP_011539532.1:p.Gln25=
XM_011541231.1:c.66G=	XP_011539533.1:p.Gln22=
XM_011541226.2:c.582G=	XP_011539528.1:p.Gln194=
XM_011541227.2:c.504G=	XP_011539529.1:p.Gln168=
XM_011541228.2:c.471G=	XP_011539530.1:p.Gln157=
XM_011541231.2:c.66G=	XP_011539533.1:p.Gln22=
XM_024446338.1:c.471G=	XP_024302106.1:p.Gln157=
NM_006623.4:c.360G= MANE Select	NP_006614.2:p.Gln120=