Canonical Allele Identifier: CA1139922774

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119743834G= , CM000663.2:g.119743834G=	GRCh38
NC_000001.10:g.120286457G= , CM000663.1:g.120286457G=	GRCh37
NC_000001.9:g.120087980G=	NCBI36
NG_009188.1:g.37039G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.1448-33G=	ENSP00000358417.5:n.1448-33G=
ENST00000641023.2:c.1448-52G= MANE Select	ENSP00000493175.1:n.1448-52G=
ENST00000641074.1:c.*27-52G=	ENSP00000493446.1:n.*27-52G=
ENST00000641115.1:c.1184-52G=	ENSP00000493264.1:n.1184-52G=
ENST00000641213.1:c.*1101-52G=	ENSP00000493079.1:n.*1101-52G=
ENST00000641314.1:n.1433-52G=
ENST00000641375.1:c.*1284-52G=	ENSP00000493089.1:n.*1284-52G=
ENST00000641597.1:c.1448-52G=	ENSP00000493382.1:n.1448-52G=
ENST00000641756.1:c.*1192-52G=	ENSP00000493147.1:n.*1192-52G=
ENST00000641811.1:c.702-52G=
ENST00000641891.1:c.*1274-52G=	ENSP00000493288.1:n.*1274-52G=
ENST00000641927.1:n.1388-52G=
ENST00000641947.1:c.1427-52G=	ENSP00000492994.1:n.1427-52G=
ENST00000642021.1:n.2479-52G=
ENST00000369407.3:c.1346-52G=	ENSP00000358415.3:n.1346-52G=
ENST00000369409.8:c.1448-52G=	ENSP00000358417.4:n.1448-52G=
ENST00000482968.1:n.1427-52G=
NM_006623.3:c.1448-52G=	NP_006614.2:n.1448-52G=
XM_011541226.1:c.1670-52G=	XP_011539528.1:n.1670-52G=
XM_011541227.1:c.1592-52G=	XP_011539529.1:n.1592-52G=
XM_011541228.1:c.1559-52G=	XP_011539530.1:n.1559-52G=
XM_011541229.1:c.1385-52G=	XP_011539531.1:n.1385-52G=
XM_011541230.1:c.1163-52G=	XP_011539532.1:n.1163-52G=
XM_011541231.1:c.1154-52G=	XP_011539533.1:n.1154-52G=
XM_011541226.2:c.1670-52G=	XP_011539528.1:n.1670-52G=
XM_011541227.2:c.1592-52G=	XP_011539529.1:n.1592-52G=
XM_011541228.2:c.1559-52G=	XP_011539530.1:n.1559-52G=
XM_011541231.2:c.1154-52G=	XP_011539533.1:n.1154-52G=
XM_024446338.1:c.1559-52G=	XP_024302106.1:n.1559-52G=
NM_006623.4:c.1448-52G= MANE Select	NP_006614.2:n.1448-52G=