Canonical Allele Identifier: CA1192431769

Gene: PHGDH

Linked Data

• dbSNP Id: rs1651451285
• gnomAD v4: 1-119726941-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119726944del , CM000663.2:g.119726944del	GRCh38
NC_000001.10:g.120269567del , CM000663.1:g.120269567del	GRCh37
NC_000001.9:g.120071090del	NCBI36
NG_009188.1:g.20149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.411+39del	ENSP00000358417.5:n.411+39del
ENST00000462324.2:n.494+39del
ENST00000641023.2:c.411+39del MANE Select	ENSP00000493175.1:n.411+39del
ENST00000641074.1:c.411+39del	ENSP00000493446.1:n.411+39del
ENST00000641115.1:c.411+39del	ENSP00000493264.1:n.411+39del
ENST00000641213.1:c.*64+39del	ENSP00000493079.1:n.*64+39del
ENST00000641247.1:c.*130+39del	ENSP00000492955.1:n.*130+39del
ENST00000641272.1:c.345+39del	ENSP00000493432.1:n.345+39del
ENST00000641314.1:n.396+39del
ENST00000641371.1:c.325+39del	ENSP00000493305.1:n.325+39del
ENST00000641375.1:c.*247+39del	ENSP00000493089.1:n.*247+39del
ENST00000641491.1:c.*64+39del	ENSP00000493187.1:n.*64+39del
ENST00000641570.1:c.*130+39del	ENSP00000493213.1:n.*130+39del
ENST00000641573.1:n.499+39del
ENST00000641587.1:c.*122+39del	ENSP00000493453.1:n.*122+39del
ENST00000641597.1:c.411+39del	ENSP00000493382.1:n.411+39del
ENST00000641711.1:n.635+39del
ENST00000641756.1:c.*155+39del	ENSP00000493147.1:n.*155+39del
ENST00000641811.1:c.167+39del
ENST00000641847.1:n.270+39del
ENST00000641891.1:c.*237+39del	ENSP00000493288.1:n.*237+39del
ENST00000641927.1:n.351+39del
ENST00000641947.1:c.411+39del	ENSP00000492994.1:n.411+39del
ENST00000642021.1:n.533+39del
ENST00000642041.1:c.*450+39del	ENSP00000493415.1:n.*450+39del
ENST00000369407.3:c.309+39del	ENSP00000358415.3:n.309+39del
ENST00000369409.8:c.411+39del	ENSP00000358417.4:n.411+39del
ENST00000462324.1:n.679+39del
ENST00000493622.5:n.600+39del
NM_006623.3:c.411+39del	NP_006614.2:n.411+39del
XM_011541226.1:c.633+39del	XP_011539528.1:n.633+39del
XM_011541227.1:c.555+39del	XP_011539529.1:n.555+39del
XM_011541228.1:c.522+39del	XP_011539530.1:n.522+39del
XM_011541229.1:c.348+39del	XP_011539531.1:n.348+39del
XM_011541230.1:c.126+39del	XP_011539532.1:n.126+39del
XM_011541231.1:c.117+39del	XP_011539533.1:n.117+39del
XM_011541226.2:c.633+39del	XP_011539528.1:n.633+39del
XM_011541227.2:c.555+39del	XP_011539529.1:n.555+39del
XM_011541228.2:c.522+39del	XP_011539530.1:n.522+39del
XM_011541231.2:c.117+39del	XP_011539533.1:n.117+39del
XM_024446338.1:c.522+39del	XP_024302106.1:n.522+39del
NM_006623.4:c.411+39del MANE Select	NP_006614.2:n.411+39del