Canonical Allele Identifier: CA341847633

Gene: PHGDH

Linked Data

• MyVariant Identifiers: chr1:g.120269523A>T (hg19) ; chr1:g.119726900A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119726900A>T , CM000663.2:g.119726900A>T	GRCh38
NC_000001.10:g.120269523A>T , CM000663.1:g.120269523A>T	GRCh37
NC_000001.9:g.120071046A>T	NCBI36
NG_009188.1:g.20105A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369409.9:c.406A>T	ENSP00000358417.5:p.Lys136Ter
ENST00000462324.2:n.489A>T
ENST00000641023.2:c.406A>T MANE Select	ENSP00000493175.1:p.Lys136Ter
ENST00000641074.1:c.406A>T	ENSP00000493446.1:p.Lys136Ter
ENST00000641115.1:c.406A>T	ENSP00000493264.1:p.Lys136Ter
ENST00000641213.1:c.*59A>T	ENSP00000493079.1:n.*59A>T
ENST00000641247.1:c.*125A>T	ENSP00000492955.1:n.*125A>T
ENST00000641272.1:c.340A>T	ENSP00000493432.1:p.Lys114Ter
ENST00000641314.1:n.391A>T
ENST00000641371.1:c.320A>T	ENSP00000493305.1:p.Glu107Val
ENST00000641375.1:c.*242A>T	ENSP00000493089.1:n.*242A>T
ENST00000641491.1:c.*59A>T	ENSP00000493187.1:n.*59A>T
ENST00000641570.1:c.*125A>T	ENSP00000493213.1:n.*125A>T
ENST00000641573.1:n.494A>T
ENST00000641587.1:c.*117A>T	ENSP00000493453.1:n.*117A>T
ENST00000641597.1:c.406A>T	ENSP00000493382.1:p.Lys136Ter
ENST00000641711.1:n.630A>T
ENST00000641756.1:c.*150A>T	ENSP00000493147.1:n.*150A>T
ENST00000641811.1:c.162A>T
ENST00000641847.1:n.265A>T
ENST00000641891.1:c.*232A>T	ENSP00000493288.1:n.*232A>T
ENST00000641927.1:n.346A>T
ENST00000641947.1:c.406A>T	ENSP00000492994.1:p.Lys136Ter
ENST00000642021.1:n.528A>T
ENST00000642041.1:c.*445A>T	ENSP00000493415.1:n.*445A>T
ENST00000369407.3:c.304A>T	ENSP00000358415.3:p.Lys102Ter
ENST00000369409.8:c.406A>T	ENSP00000358417.4:p.Lys136Ter
ENST00000462324.1:n.674A>T
ENST00000493622.5:n.595A>T
NM_006623.3:c.406A>T	NP_006614.2:p.Lys136Ter
XM_011541226.1:c.628A>T	XP_011539528.1:p.Lys210Ter
XM_011541227.1:c.550A>T	XP_011539529.1:p.Lys184Ter
XM_011541228.1:c.517A>T	XP_011539530.1:p.Lys173Ter
XM_011541229.1:c.343A>T	XP_011539531.1:p.Lys115Ter
XM_011541230.1:c.121A>T	XP_011539532.1:p.Lys41Ter
XM_011541231.1:c.112A>T	XP_011539533.1:p.Lys38Ter
XM_011541226.2:c.628A>T	XP_011539528.1:p.Lys210Ter
XM_011541227.2:c.550A>T	XP_011539529.1:p.Lys184Ter
XM_011541228.2:c.517A>T	XP_011539530.1:p.Lys173Ter
XM_011541231.2:c.112A>T	XP_011539533.1:p.Lys38Ter
XM_024446338.1:c.517A>T	XP_024302106.1:p.Lys173Ter
NM_006623.4:c.406A>T MANE Select	NP_006614.2:p.Lys136Ter