Canonical Allele Identifier: CA1192434164

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119743911G= , CM000663.2:g.119743911G=	GRCh38
NC_000001.10:g.120286534G= , CM000663.1:g.120286534G=	GRCh37
NC_000001.9:g.120088057G=	NCBI36
NG_009188.1:g.37116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.1492G=	ENSP00000358417.5:p.Ala498=
ENST00000641023.2:c.1473G= MANE Select	ENSP00000493175.1:p.Arg491=
ENST00000641074.1:c.*52G=	ENSP00000493446.1:n.*52G=
ENST00000641115.1:c.1209G=	ENSP00000493264.1:p.Arg403=
ENST00000641213.1:c.*1126G=	ENSP00000493079.1:n.*1126G=
ENST00000641314.1:n.1458G=
ENST00000641375.1:c.*1309G=	ENSP00000493089.1:n.*1309G=
ENST00000641597.1:c.1473G=	ENSP00000493382.1:p.Arg491=
ENST00000641756.1:c.*1217G=	ENSP00000493147.1:n.*1217G=
ENST00000641811.1:c.727G=
ENST00000641891.1:c.*1299G=	ENSP00000493288.1:n.*1299G=
ENST00000641927.1:n.1413G=
ENST00000641947.1:c.1452G=	ENSP00000492994.1:p.Arg484=
ENST00000642021.1:n.2504G=
ENST00000369407.3:c.1371G=	ENSP00000358415.3:p.Arg457=
ENST00000369409.8:c.1473G=	ENSP00000358417.4:p.Arg491=
ENST00000482968.1:n.1452G=
NM_006623.3:c.1473G=	NP_006614.2:p.Arg491=
XM_011541226.1:c.1695G=	XP_011539528.1:p.Arg565=
XM_011541227.1:c.1617G=	XP_011539529.1:p.Arg539=
XM_011541228.1:c.1584G=	XP_011539530.1:p.Arg528=
XM_011541229.1:c.1410G=	XP_011539531.1:p.Arg470=
XM_011541230.1:c.1188G=	XP_011539532.1:p.Arg396=
XM_011541231.1:c.1179G=	XP_011539533.1:p.Arg393=
XM_011541226.2:c.1695G=	XP_011539528.1:p.Arg565=
XM_011541227.2:c.1617G=	XP_011539529.1:p.Arg539=
XM_011541228.2:c.1584G=	XP_011539530.1:p.Arg528=
XM_011541231.2:c.1179G=	XP_011539533.1:p.Arg393=
XM_024446338.1:c.1584G=	XP_024302106.1:p.Arg528=
NM_006623.4:c.1473G= MANE Select	NP_006614.2:p.Arg491=