Canonical Allele Identifier: CA1192431829

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727084G= , CM000663.2:g.119727084G=	GRCh38
NC_000001.10:g.120269707G= , CM000663.1:g.120269707G=	GRCh37
NC_000001.9:g.120071230G=	NCBI36
NG_009188.1:g.20289G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.492G=	ENSP00000358417.5:p.Met164=
ENST00000462324.2:n.575G=
ENST00000641023.2:c.492G= MANE Select	ENSP00000493175.1:p.Met164=
ENST00000641074.1:c.492G=	ENSP00000493446.1:p.Met164=
ENST00000641115.1:c.492G=	ENSP00000493264.1:p.Met164=
ENST00000641213.1:c.*145G=	ENSP00000493079.1:n.*145G=
ENST00000641247.1:c.*211G=	ENSP00000492955.1:n.*211G=
ENST00000641272.1:c.426G=	ENSP00000493432.1:p.Met142=
ENST00000641314.1:n.477G=
ENST00000641371.1:c.406G=	ENSP00000493305.1:p.Ala136=
ENST00000641375.1:c.*328G=	ENSP00000493089.1:n.*328G=
ENST00000641455.1:n.37G=
ENST00000641491.1:c.*145G=	ENSP00000493187.1:n.*145G=
ENST00000641570.1:c.*211G=	ENSP00000493213.1:n.*211G=
ENST00000641573.1:n.580G=
ENST00000641587.1:c.*203G=	ENSP00000493453.1:n.*203G=
ENST00000641597.1:c.492G=	ENSP00000493382.1:p.Met164=
ENST00000641756.1:c.*236G=	ENSP00000493147.1:n.*236G=
ENST00000641811.1:c.248G=
ENST00000641847.1:n.351G=
ENST00000641891.1:c.*318G=	ENSP00000493288.1:n.*318G=
ENST00000641927.1:n.432G=
ENST00000641947.1:c.492G=	ENSP00000492994.1:p.Met164=
ENST00000642021.1:n.614G=
ENST00000369407.3:c.390G=	ENSP00000358415.3:p.Met130=
ENST00000369409.8:c.492G=	ENSP00000358417.4:p.Met164=
ENST00000462324.1:n.760G=
ENST00000493622.5:n.681G=
NM_006623.3:c.492G=	NP_006614.2:p.Met164=
XM_011541226.1:c.714G=	XP_011539528.1:p.Met238=
XM_011541227.1:c.636G=	XP_011539529.1:p.Met212=
XM_011541228.1:c.603G=	XP_011539530.1:p.Met201=
XM_011541229.1:c.429G=	XP_011539531.1:p.Met143=
XM_011541230.1:c.207G=	XP_011539532.1:p.Met69=
XM_011541231.1:c.198G=	XP_011539533.1:p.Met66=
XM_011541226.2:c.714G=	XP_011539528.1:p.Met238=
XM_011541227.2:c.636G=	XP_011539529.1:p.Met212=
XM_011541228.2:c.603G=	XP_011539530.1:p.Met201=
XM_011541231.2:c.198G=	XP_011539533.1:p.Met66=
XM_024446338.1:c.603G=	XP_024302106.1:p.Met201=
NM_006623.4:c.492G= MANE Select	NP_006614.2:p.Met164=