Canonical Allele Identifier: CA10685757

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119742046A>T , CM000663.2:g.119742046A>T	GRCh38
NC_000001.10:g.120284669A>T , CM000663.1:g.120284669A>T	GRCh37
NC_000001.9:g.120086192A>T	NCBI36
NG_009188.1:g.35251A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.1209+149A>T	ENSP00000358417.5:n.1209+149A>T
ENST00000641023.2:c.1209+149A>T MANE Select	ENSP00000493175.1:n.1209+149A>T
ENST00000641074.1:c.1079-761A>T	ENSP00000493446.1:n.1079-761A>T
ENST00000641115.1:c.946-761A>T	ENSP00000493264.1:n.946-761A>T
ENST00000641213.1:c.*862+149A>T	ENSP00000493079.1:n.*862+149A>T
ENST00000641314.1:n.1194+149A>T
ENST00000641375.1:c.*1045+149A>T	ENSP00000493089.1:n.*1045+149A>T
ENST00000641597.1:c.1209+149A>T	ENSP00000493382.1:n.1209+149A>T
ENST00000641756.1:c.*953+149A>T	ENSP00000493147.1:n.*953+149A>T
ENST00000641811.1:c.702-1840A>T
ENST00000641891.1:c.*1035+149A>T	ENSP00000493288.1:n.*1035+149A>T
ENST00000641927.1:n.1149+149A>T
ENST00000641939.1:n.312+149A>T
ENST00000641947.1:c.1188+170A>T	ENSP00000492994.1:n.1188+170A>T
ENST00000642021.1:n.1480A>T
ENST00000369407.3:c.1107+149A>T	ENSP00000358415.3:n.1107+149A>T
ENST00000369409.8:c.1209+149A>T	ENSP00000358417.4:n.1209+149A>T
ENST00000482968.1:n.1188+149A>T
NM_006623.3:c.1209+149A>T	NP_006614.2:n.1209+149A>T
XM_011541226.1:c.1431+149A>T	XP_011539528.1:n.1431+149A>T
XM_011541227.1:c.1353+149A>T	XP_011539529.1:n.1353+149A>T
XM_011541228.1:c.1320+149A>T	XP_011539530.1:n.1320+149A>T
XM_011541229.1:c.1146+149A>T	XP_011539531.1:n.1146+149A>T
XM_011541230.1:c.924+149A>T	XP_011539532.1:n.924+149A>T
XM_011541231.1:c.915+149A>T	XP_011539533.1:n.915+149A>T
XM_011541226.2:c.1431+149A>T	XP_011539528.1:n.1431+149A>T
XM_011541227.2:c.1353+149A>T	XP_011539529.1:n.1353+149A>T
XM_011541228.2:c.1320+149A>T	XP_011539530.1:n.1320+149A>T
XM_011541231.2:c.915+149A>T	XP_011539533.1:n.915+149A>T
XM_024446338.1:c.1320+149A>T	XP_024302106.1:n.1320+149A>T
NM_006623.4:c.1209+149A>T MANE Select	NP_006614.2:n.1209+149A>T