Canonical Allele Identifier: CA10927403

Gene: PHGDH

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119714953A>G , CM000663.2:g.119714953A>G	GRCh38
NC_000001.10:g.120257576A>G , CM000663.1:g.120257576A>G	GRCh37
NC_000001.9:g.120059099A>G	NCBI36
NG_009188.1:g.8158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.138+2793A>G	ENSP00000358417.5:n.138+2793A>G
ENST00000462324.2:n.221+2793A>G
ENST00000496756.2:n.274+2793A>G
ENST00000641023.2:c.138+2793A>G MANE Select	ENSP00000493175.1:n.138+2793A>G
ENST00000641074.1:c.138+2793A>G	ENSP00000493446.1:n.138+2793A>G
ENST00000641115.1:c.138+2793A>G	ENSP00000493264.1:n.138+2793A>G
ENST00000641213.1:c.138+2793A>G	ENSP00000493079.1:n.138+2793A>G
ENST00000641247.1:c.138+2793A>G	ENSP00000492955.1:n.138+2793A>G
ENST00000641272.1:c.138+2793A>G	ENSP00000493432.1:n.138+2793A>G
ENST00000641371.1:c.138+2793A>G	ENSP00000493305.1:n.138+2793A>G
ENST00000641375.1:c.138+2793A>G	ENSP00000493089.1:n.138+2793A>G
ENST00000641491.1:c.138+2793A>G	ENSP00000493187.1:n.138+2793A>G
ENST00000641513.1:c.138+2793A>G	ENSP00000493398.1:n.138+2793A>G
ENST00000641570.1:c.138+2793A>G	ENSP00000493213.1:n.138+2793A>G
ENST00000641573.1:n.226+2793A>G
ENST00000641587.1:c.138+2793A>G	ENSP00000493453.1:n.138+2793A>G
ENST00000641597.1:c.138+2793A>G	ENSP00000493382.1:n.138+2793A>G
ENST00000641711.1:n.362+1493A>G
ENST00000641720.1:c.138+2793A>G	ENSP00000492948.1:n.138+2793A>G
ENST00000641756.1:c.-148+1776A>G	ENSP00000493147.1:n.-148+1776A>G
ENST00000641891.1:c.138+2793A>G	ENSP00000493288.1:n.138+2793A>G
ENST00000641927.1:n.78+465A>G
ENST00000641947.1:c.138+2793A>G	ENSP00000492994.1:n.138+2793A>G
ENST00000642021.1:n.260+2793A>G
ENST00000642041.1:c.138+2793A>G	ENSP00000493415.1:n.138+2793A>G
ENST00000369409.8:c.138+2793A>G	ENSP00000358417.4:n.138+2793A>G
ENST00000462324.1:n.255+2793A>G
ENST00000493622.5:n.328-6217A>G
ENST00000496756.1:n.277+2793A>G
NM_006623.3:c.138+2793A>G	NP_006614.2:n.138+2793A>G
XM_011541226.1:c.138+2793A>G	XP_011539528.1:n.138+2793A>G
XM_011541227.1:c.60+2095A>G	XP_011539529.1:n.60+2095A>G
XM_011541229.1:c.-148+1493A>G	XP_011539531.1:n.-148+1493A>G
XM_011541230.1:c.-148+1493A>G	XP_011539532.1:n.-148+1493A>G
XM_011541231.1:c.-399+2793A>G	XP_011539533.1:n.-399+2793A>G
XM_011541226.2:c.138+2793A>G	XP_011539528.1:n.138+2793A>G
XM_011541227.2:c.60+2095A>G	XP_011539529.1:n.60+2095A>G
XM_011541228.2:c.-4940A>G	XP_011539530.1:n.-4940A>G
XM_011541231.2:c.-399+2793A>G	XP_011539533.1:n.-399+2793A>G
XM_024446338.1:c.-4643A>G	XP_024302106.1:n.-4643A>G
NM_006623.4:c.138+2793A>G MANE Select	NP_006614.2:n.138+2793A>G