Canonical Allele Identifier: CA420012769

Gene: PHGDH

Linked Data

• MyVariant Identifiers: chr1:g.120269635A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727012A>T , CM000663.2:g.119727012A>T	GRCh38
NC_000001.10:g.120269635A>T , CM000663.1:g.120269635A>T	GRCh37
NC_000001.9:g.120071158A>T	NCBI36
NG_009188.1:g.20217A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.420A>T	ENSP00000358417.5:p.Gly140=
ENST00000462324.2:n.503A>T
ENST00000641023.2:c.420A>T MANE Select	ENSP00000493175.1:p.Gly140=
ENST00000641074.1:c.420A>T	ENSP00000493446.1:p.Gly140=
ENST00000641115.1:c.420A>T	ENSP00000493264.1:p.Gly140=
ENST00000641213.1:c.*73A>T	ENSP00000493079.1:n.*73A>T
ENST00000641247.1:c.*139A>T	ENSP00000492955.1:n.*139A>T
ENST00000641272.1:c.354A>T	ENSP00000493432.1:p.Gly118=
ENST00000641314.1:n.405A>T
ENST00000641371.1:c.334A>T	ENSP00000493305.1:p.Asn112Tyr
ENST00000641375.1:c.*256A>T	ENSP00000493089.1:n.*256A>T
ENST00000641491.1:c.*73A>T	ENSP00000493187.1:n.*73A>T
ENST00000641570.1:c.*139A>T	ENSP00000493213.1:n.*139A>T
ENST00000641573.1:n.508A>T
ENST00000641587.1:c.*131A>T	ENSP00000493453.1:n.*131A>T
ENST00000641597.1:c.420A>T	ENSP00000493382.1:p.Gly140=
ENST00000641711.1:n.644A>T
ENST00000641756.1:c.*164A>T	ENSP00000493147.1:n.*164A>T
ENST00000641811.1:c.176A>T
ENST00000641847.1:n.279A>T
ENST00000641891.1:c.*246A>T	ENSP00000493288.1:n.*246A>T
ENST00000641927.1:n.360A>T
ENST00000641947.1:c.420A>T	ENSP00000492994.1:p.Gly140=
ENST00000642021.1:n.542A>T
ENST00000642041.1:c.*459A>T	ENSP00000493415.1:n.*459A>T
ENST00000369407.3:c.318A>T	ENSP00000358415.3:p.Gly106=
ENST00000369409.8:c.420A>T	ENSP00000358417.4:p.Gly140=
ENST00000462324.1:n.688A>T
ENST00000493622.5:n.609A>T
NM_006623.3:c.420A>T	NP_006614.2:p.Gly140=
XM_011541226.1:c.642A>T	XP_011539528.1:p.Gly214=
XM_011541227.1:c.564A>T	XP_011539529.1:p.Gly188=
XM_011541228.1:c.531A>T	XP_011539530.1:p.Gly177=
XM_011541229.1:c.357A>T	XP_011539531.1:p.Gly119=
XM_011541230.1:c.135A>T	XP_011539532.1:p.Gly45=
XM_011541231.1:c.126A>T	XP_011539533.1:p.Gly42=
XM_011541226.2:c.642A>T	XP_011539528.1:p.Gly214=
XM_011541227.2:c.564A>T	XP_011539529.1:p.Gly188=
XM_011541228.2:c.531A>T	XP_011539530.1:p.Gly177=
XM_011541231.2:c.126A>T	XP_011539533.1:p.Gly42=
XM_024446338.1:c.531A>T	XP_024302106.1:p.Gly177=
NM_006623.4:c.420A>T MANE Select	NP_006614.2:p.Gly140=