Canonical Allele Identifier: CA420017149

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119743917G>C , CM000663.2:g.119743917G>C	GRCh38
NC_000001.10:g.120286540G>C , CM000663.1:g.120286540G>C	GRCh37
NC_000001.9:g.120088063G>C	NCBI36
NG_009188.1:g.37122G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006623.4:c.1479G>C MANE Select	NP_006614.2:p.Leu493=
ENST00000641023.2:c.1479G>C MANE Select	ENSP00000493175.1:p.Leu493=
NM_006623.3:c.1479G>C	NP_006614.2:p.Leu493=
ENST00000369407.3:c.1377G>C	ENSP00000358415.3:p.Leu459=
ENST00000369409.8:c.1479G>C	ENSP00000358417.4:p.Leu493=
ENST00000369409.9:c.1498G>C	ENSP00000358417.5:p.Val500Leu
ENST00000482968.1:n.1458G>C
ENST00000641074.1:c.*58G>C	ENSP00000493446.1:n.*58G>C
ENST00000641115.1:c.1215G>C	ENSP00000493264.1:p.Leu405=
ENST00000641213.1:c.*1132G>C	ENSP00000493079.1:n.*1132G>C
ENST00000641314.1:n.1464G>C
ENST00000641375.1:c.*1315G>C	ENSP00000493089.1:n.*1315G>C
ENST00000641597.1:c.1479G>C	ENSP00000493382.1:p.Leu493=
ENST00000641756.1:c.*1223G>C	ENSP00000493147.1:n.*1223G>C
ENST00000641811.1:c.733G>C
ENST00000641891.1:c.*1305G>C	ENSP00000493288.1:n.*1305G>C
ENST00000641927.1:n.1419G>C
ENST00000641947.1:c.1458G>C	ENSP00000492994.1:p.Leu486=
ENST00000642021.1:n.2510G>C
XM_011541226.1:c.1701G>C	XP_011539528.1:p.Leu567=
XM_011541226.2:c.1701G>C	XP_011539528.1:p.Leu567=
XM_011541227.1:c.1623G>C	XP_011539529.1:p.Leu541=
XM_011541227.2:c.1623G>C	XP_011539529.1:p.Leu541=
XM_011541228.1:c.1590G>C	XP_011539530.1:p.Leu530=
XM_011541228.2:c.1590G>C	XP_011539530.1:p.Leu530=
XM_011541229.1:c.1416G>C	XP_011539531.1:p.Leu472=
XM_011541230.1:c.1194G>C	XP_011539532.1:p.Leu398=
XM_011541231.1:c.1185G>C	XP_011539533.1:p.Leu395=
XM_011541231.2:c.1185G>C	XP_011539533.1:p.Leu395=
XM_024446338.1:c.1590G>C	XP_024302106.1:p.Leu530=