Canonical Allele Identifier: CA1192431819

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727059T= , CM000663.2:g.119727059T=	GRCh38
NC_000001.10:g.120269682T= , CM000663.1:g.120269682T=	GRCh37
NC_000001.9:g.120071205T=	NCBI36
NG_009188.1:g.20264T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.467T=	ENSP00000358417.5:p.Ile156=
ENST00000462324.2:n.550T=
ENST00000641023.2:c.467T= MANE Select	ENSP00000493175.1:p.Ile156=
ENST00000641074.1:c.467T=	ENSP00000493446.1:p.Ile156=
ENST00000641115.1:c.467T=	ENSP00000493264.1:p.Ile156=
ENST00000641213.1:c.*120T=	ENSP00000493079.1:n.*120T=
ENST00000641247.1:c.*186T=	ENSP00000492955.1:n.*186T=
ENST00000641272.1:c.401T=	ENSP00000493432.1:p.Ile134=
ENST00000641314.1:n.452T=
ENST00000641371.1:c.381T=	ENSP00000493305.1:p.Asp127=
ENST00000641375.1:c.*303T=	ENSP00000493089.1:n.*303T=
ENST00000641455.1:n.12T=
ENST00000641491.1:c.*120T=	ENSP00000493187.1:n.*120T=
ENST00000641570.1:c.*186T=	ENSP00000493213.1:n.*186T=
ENST00000641573.1:n.555T=
ENST00000641587.1:c.*178T=	ENSP00000493453.1:n.*178T=
ENST00000641597.1:c.467T=	ENSP00000493382.1:p.Ile156=
ENST00000641711.1:n.691T=
ENST00000641756.1:c.*211T=	ENSP00000493147.1:n.*211T=
ENST00000641811.1:c.223T=
ENST00000641847.1:n.326T=
ENST00000641891.1:c.*293T=	ENSP00000493288.1:n.*293T=
ENST00000641927.1:n.407T=
ENST00000641947.1:c.467T=	ENSP00000492994.1:p.Ile156=
ENST00000642021.1:n.589T=
ENST00000642041.1:c.*506T=	ENSP00000493415.1:n.*506T=
ENST00000369407.3:c.365T=	ENSP00000358415.3:p.Ile122=
ENST00000369409.8:c.467T=	ENSP00000358417.4:p.Ile156=
ENST00000462324.1:n.735T=
ENST00000493622.5:n.656T=
NM_006623.3:c.467T=	NP_006614.2:p.Ile156=
XM_011541226.1:c.689T=	XP_011539528.1:p.Ile230=
XM_011541227.1:c.611T=	XP_011539529.1:p.Ile204=
XM_011541228.1:c.578T=	XP_011539530.1:p.Ile193=
XM_011541229.1:c.404T=	XP_011539531.1:p.Ile135=
XM_011541230.1:c.182T=	XP_011539532.1:p.Ile61=
XM_011541231.1:c.173T=	XP_011539533.1:p.Ile58=
XM_011541226.2:c.689T=	XP_011539528.1:p.Ile230=
XM_011541227.2:c.611T=	XP_011539529.1:p.Ile204=
XM_011541228.2:c.578T=	XP_011539530.1:p.Ile193=
XM_011541231.2:c.173T=	XP_011539533.1:p.Ile58=
XM_024446338.1:c.578T=	XP_024302106.1:p.Ile193=
NM_006623.4:c.467T= MANE Select	NP_006614.2:p.Ile156=