Canonical Allele Identifier: CA341847827

Gene: PHGDH

Linked Data

• MyVariant Identifiers: chr1:g.120269709A>T (hg19) ; chr1:g.119727086A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727086A>T , CM000663.2:g.119727086A>T	GRCh38
NC_000001.10:g.120269709A>T , CM000663.1:g.120269709A>T	GRCh37
NC_000001.9:g.120071232A>T	NCBI36
NG_009188.1:g.20291A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.494A>T	ENSP00000358417.5:p.Gln165Leu
ENST00000462324.2:n.577A>T
ENST00000641023.2:c.494A>T MANE Select	ENSP00000493175.1:p.Gln165Leu
ENST00000641074.1:c.494A>T	ENSP00000493446.1:p.Gln165Leu
ENST00000641115.1:c.494A>T	ENSP00000493264.1:p.Gln165Leu
ENST00000641213.1:c.*147A>T	ENSP00000493079.1:n.*147A>T
ENST00000641247.1:c.*213A>T	ENSP00000492955.1:n.*213A>T
ENST00000641272.1:c.428A>T	ENSP00000493432.1:p.Gln143Leu
ENST00000641314.1:n.479A>T
ENST00000641371.1:c.408A>T	ENSP00000493305.1:p.Ala136=
ENST00000641375.1:c.*330A>T	ENSP00000493089.1:n.*330A>T
ENST00000641455.1:n.39A>T
ENST00000641491.1:c.*147A>T	ENSP00000493187.1:n.*147A>T
ENST00000641570.1:c.*213A>T	ENSP00000493213.1:n.*213A>T
ENST00000641573.1:n.582A>T
ENST00000641587.1:c.*205A>T	ENSP00000493453.1:n.*205A>T
ENST00000641597.1:c.494A>T	ENSP00000493382.1:p.Gln165Leu
ENST00000641756.1:c.*238A>T	ENSP00000493147.1:n.*238A>T
ENST00000641811.1:c.250A>T
ENST00000641847.1:n.353A>T
ENST00000641891.1:c.*320A>T	ENSP00000493288.1:n.*320A>T
ENST00000641927.1:n.434A>T
ENST00000641947.1:c.494A>T	ENSP00000492994.1:p.Gln165Leu
ENST00000642021.1:n.616A>T
ENST00000369407.3:c.392A>T	ENSP00000358415.3:p.Gln131Leu
ENST00000369409.8:c.494A>T	ENSP00000358417.4:p.Gln165Leu
ENST00000462324.1:n.762A>T
ENST00000493622.5:n.683A>T
NM_006623.3:c.494A>T	NP_006614.2:p.Gln165Leu
XM_011541226.1:c.716A>T	XP_011539528.1:p.Gln239Leu
XM_011541227.1:c.638A>T	XP_011539529.1:p.Gln213Leu
XM_011541228.1:c.605A>T	XP_011539530.1:p.Gln202Leu
XM_011541229.1:c.431A>T	XP_011539531.1:p.Gln144Leu
XM_011541230.1:c.209A>T	XP_011539532.1:p.Gln70Leu
XM_011541231.1:c.200A>T	XP_011539533.1:p.Gln67Leu
XM_011541226.2:c.716A>T	XP_011539528.1:p.Gln239Leu
XM_011541227.2:c.638A>T	XP_011539529.1:p.Gln213Leu
XM_011541228.2:c.605A>T	XP_011539530.1:p.Gln202Leu
XM_011541231.2:c.200A>T	XP_011539533.1:p.Gln67Leu
XM_024446338.1:c.605A>T	XP_024302106.1:p.Gln202Leu
NM_006623.4:c.494A>T MANE Select	NP_006614.2:p.Gln165Leu