Canonical Allele Identifier: CA2992704373

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119743823_119743825dup , CM000663.2:g.119743823_119743825dup	GRCh38
NC_000001.10:g.120286446_120286448dup , CM000663.1:g.120286446_120286448dup	GRCh37
NC_000001.9:g.120087969_120087971dup	NCBI36
NG_009188.1:g.37028_37030dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.1448-44_1448-42dup	ENSP00000358417.5:n.1448-44_1448-42dup
ENST00000641023.2:c.1448-63_1448-61dup MANE Select	ENSP00000493175.1:n.1448-63_1448-61dup
ENST00000641074.1:c.*27-63_*27-61dup	ENSP00000493446.1:n.*27-63_*27-61dup
ENST00000641115.1:c.1184-63_1184-61dup	ENSP00000493264.1:n.1184-63_1184-61dup
ENST00000641213.1:c.*1101-63_*1101-61dup	ENSP00000493079.1:n.*1101-63_*1101-61dup
ENST00000641314.1:n.1433-63_1433-61dup
ENST00000641375.1:c.*1284-63_*1284-61dup	ENSP00000493089.1:n.*1284-63_*1284-61dup
ENST00000641597.1:c.1448-63_1448-61dup	ENSP00000493382.1:n.1448-63_1448-61dup
ENST00000641756.1:c.*1192-63_*1192-61dup	ENSP00000493147.1:n.*1192-63_*1192-61dup
ENST00000641811.1:c.702-63_702-61dup
ENST00000641891.1:c.*1274-63_*1274-61dup	ENSP00000493288.1:n.*1274-63_*1274-61dup
ENST00000641927.1:n.1388-63_1388-61dup
ENST00000641947.1:c.1427-63_1427-61dup	ENSP00000492994.1:n.1427-63_1427-61dup
ENST00000642021.1:n.2479-63_2479-61dup
ENST00000369407.3:c.1346-63_1346-61dup	ENSP00000358415.3:n.1346-63_1346-61dup
ENST00000369409.8:c.1448-63_1448-61dup	ENSP00000358417.4:n.1448-63_1448-61dup
ENST00000482968.1:n.1427-63_1427-61dup
NM_006623.3:c.1448-63_1448-61dup	NP_006614.2:n.1448-63_1448-61dup
XM_011541226.1:c.1670-63_1670-61dup	XP_011539528.1:n.1670-63_1670-61dup
XM_011541227.1:c.1592-63_1592-61dup	XP_011539529.1:n.1592-63_1592-61dup
XM_011541228.1:c.1559-63_1559-61dup	XP_011539530.1:n.1559-63_1559-61dup
XM_011541229.1:c.1385-63_1385-61dup	XP_011539531.1:n.1385-63_1385-61dup
XM_011541230.1:c.1163-63_1163-61dup	XP_011539532.1:n.1163-63_1163-61dup
XM_011541231.1:c.1154-63_1154-61dup	XP_011539533.1:n.1154-63_1154-61dup
XM_011541226.2:c.1670-63_1670-61dup	XP_011539528.1:n.1670-63_1670-61dup
XM_011541227.2:c.1592-63_1592-61dup	XP_011539529.1:n.1592-63_1592-61dup
XM_011541228.2:c.1559-63_1559-61dup	XP_011539530.1:n.1559-63_1559-61dup
XM_011541231.2:c.1154-63_1154-61dup	XP_011539533.1:n.1154-63_1154-61dup
XM_024446338.1:c.1559-63_1559-61dup	XP_024302106.1:n.1559-63_1559-61dup
NM_006623.4:c.1448-63_1448-61dup MANE Select	NP_006614.2:n.1448-63_1448-61dup