Canonical Allele Identifier: CA2992704359
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119743819T>A , CM000663.2:g.119743819T>A GRCh38
NC_000001.10:g.120286442T>A , CM000663.1:g.120286442T>A GRCh37
NC_000001.9:g.120087965T>A NCBI36
NG_009188.1:g.37024T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.1448-48T>A ENSP00000358417.5:n.1448-48T>A
ENST00000641023.2:c.1448-67T>A MANE Select ENSP00000493175.1:n.1448-67T>A
ENST00000641074.1:c.*27-67T>A ENSP00000493446.1:n.*27-67T>A
ENST00000641115.1:c.1184-67T>A ENSP00000493264.1:n.1184-67T>A
ENST00000641213.1:c.*1101-67T>A ENSP00000493079.1:n.*1101-67T>A
ENST00000641314.1:n.1433-67T>A
ENST00000641375.1:c.*1284-67T>A ENSP00000493089.1:n.*1284-67T>A
ENST00000641597.1:c.1448-67T>A ENSP00000493382.1:n.1448-67T>A
ENST00000641756.1:c.*1192-67T>A ENSP00000493147.1:n.*1192-67T>A
ENST00000641811.1:c.702-67T>A
ENST00000641891.1:c.*1274-67T>A ENSP00000493288.1:n.*1274-67T>A
ENST00000641927.1:n.1388-67T>A
ENST00000641947.1:c.1427-67T>A ENSP00000492994.1:n.1427-67T>A
ENST00000642021.1:n.2479-67T>A
ENST00000369407.3:c.1346-67T>A ENSP00000358415.3:n.1346-67T>A
ENST00000369409.8:c.1448-67T>A ENSP00000358417.4:n.1448-67T>A
ENST00000482968.1:n.1427-67T>A
NM_006623.3:c.1448-67T>A NP_006614.2:n.1448-67T>A
XM_011541226.1:c.1670-67T>A XP_011539528.1:n.1670-67T>A
XM_011541227.1:c.1592-67T>A XP_011539529.1:n.1592-67T>A
XM_011541228.1:c.1559-67T>A XP_011539530.1:n.1559-67T>A
XM_011541229.1:c.1385-67T>A XP_011539531.1:n.1385-67T>A
XM_011541230.1:c.1163-67T>A XP_011539532.1:n.1163-67T>A
XM_011541231.1:c.1154-67T>A XP_011539533.1:n.1154-67T>A
XM_011541226.2:c.1670-67T>A XP_011539528.1:n.1670-67T>A
XM_011541227.2:c.1592-67T>A XP_011539529.1:n.1592-67T>A
XM_011541228.2:c.1559-67T>A XP_011539530.1:n.1559-67T>A
XM_011541231.2:c.1154-67T>A XP_011539533.1:n.1154-67T>A
XM_024446338.1:c.1559-67T>A XP_024302106.1:n.1559-67T>A
NM_006623.4:c.1448-67T>A MANE Select NP_006614.2:n.1448-67T>A