Canonical Allele Identifier: CA10624905

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140221540C>T , CM000670.2:g.140221540C>T	GRCh38
NC_000008.10:g.141231639C>T , CM000670.1:g.141231639C>T	GRCh37
NC_000008.9:g.141300821C>T	NCBI36
NG_016478.2:g.242040G>A
NG_016478.3:g.242040G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.2475G>A MANE Select	ENSP00000405060.3:p.Arg825=
ENST00000648948.2:c.2475G>A	ENSP00000498020.1:p.Arg825=
ENST00000389328.8:c.2769G>A	ENSP00000373979.4:p.Arg923=
ENST00000438773.2:c.2475G>A	ENSP00000405060.2:p.Arg825=
ENST00000517667.5:n.197G>A
ENST00000518839.1:n.321G>A
ENST00000520532.5:n.322G>A
ENST00000520857.5:c.2005G>A
ENST00000521667.5:n.880G>A
NM_001160372.2:c.2475G>A	NP_001153844.1:p.Arg825=
NM_031466.6:c.2769G>A	NP_113654.4:p.Arg923=
XM_005251077.3:c.2475G>A	XP_005251134.1:p.Arg825=
XM_011517326.1:c.2742G>A	XP_011515628.1:p.Arg914=
XM_011517327.1:c.2769G>A	XP_011515629.1:p.Arg923=
XM_011517328.1:c.2769G>A	XP_011515630.1:p.Arg923=
XM_011517329.1:c.1863G>A	XP_011515631.1:p.Arg621=
XM_011517330.1:c.924G>A	XP_011515632.1:p.Arg308=
XR_928355.1:n.2784G>A
NM_001160372.3:c.2475G>A	NP_001153844.1:p.Arg825=
NM_001321646.1:c.2448G>A	NP_001308575.1:p.Arg816=
NM_031466.7:c.2769G>A	NP_113654.4:p.Arg923=
XM_011517326.2:c.2742G>A	XP_011515628.1:p.Arg914=
XM_011517328.2:c.2769G>A	XP_011515630.1:p.Arg923=
XM_011517330.2:c.924G>A	XP_011515632.1:p.Arg308=
XM_017013893.1:c.2769G>A	XP_016869382.1:p.Arg923=
XM_017013894.2:c.1095G>A	XP_016869383.1:p.Arg365=
XR_928355.2:n.2784G>A
NM_001160372.4:c.2475G>A MANE Select	NP_001153844.1:p.Arg825=
NM_001321646.2:c.2448G>A	NP_001308575.1:p.Arg816=
NM_001374682.1:c.2496G>A	NP_001361611.1:p.Arg832=
NM_001374683.1:c.2475G>A	NP_001361612.1:p.Arg825=
NM_001374684.1:c.2331G>A	NP_001361613.1:p.Arg777=
NM_031466.8:c.2475G>A	NP_113654.5:p.Arg825=
NR_164662.1:n.2564G>A