Canonical Allele Identifier: CA372735284

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139910191G>C , CM000670.2:g.139910191G>C	GRCh38
NC_000008.10:g.140922435G>C , CM000670.1:g.140922435G>C	GRCh37
NC_000008.9:g.140991617G>C	NCBI36
NG_016478.2:g.553389C>G
NG_016478.3:g.553389C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001160372.4:c.2920C>G MANE Select	NP_001153844.1:p.Arg974Gly
ENST00000438773.4:c.2920C>G MANE Select	ENSP00000405060.3:p.Arg974Gly
NM_001160372.2:c.2920C>G	NP_001153844.1:p.Arg974Gly
NM_001160372.3:c.2920C>G	NP_001153844.1:p.Arg974Gly
NM_001321646.1:c.2893C>G	NP_001308575.1:p.Arg965Gly
NM_001321646.2:c.2893C>G	NP_001308575.1:p.Arg965Gly
NM_001374682.1:c.2941C>G	NP_001361611.1:p.Arg981Gly
NM_001374683.1:c.2809C>G	NP_001361612.1:p.Arg937Gly
NM_001374684.1:c.2776C>G	NP_001361613.1:p.Arg926Gly
NM_031466.6:c.3214C>G	NP_113654.4:p.Arg1072Gly
NM_031466.7:c.3214C>G	NP_113654.4:p.Arg1072Gly
NM_031466.8:c.2920C>G	NP_113654.5:p.Arg974Gly
NR_164662.1:n.3009C>G
ENST00000389328.8:c.3214C>G	ENSP00000373979.4:p.Arg1072Gly
ENST00000438773.2:c.2920C>G	ENSP00000405060.2:p.Arg974Gly
ENST00000520857.5:c.2450C>G
ENST00000521667.5:n.1325C>G
ENST00000523777.5:n.529C>G
ENST00000524162.5:n.346C>G
ENST00000648948.2:c.2920C>G	ENSP00000498020.1:p.Arg974Gly
XM_005251077.3:c.2920C>G	XP_005251134.1:p.Arg974Gly
XM_011517326.1:c.3187C>G	XP_011515628.1:p.Arg1063Gly
XM_011517326.2:c.3187C>G	XP_011515628.1:p.Arg1063Gly
XM_011517327.1:c.3214C>G	XP_011515629.1:p.Arg1072Gly
XM_011517328.1:c.3214C>G	XP_011515630.1:p.Arg1072Gly
XM_011517328.2:c.3214C>G	XP_011515630.1:p.Arg1072Gly
XM_011517329.1:c.2308C>G	XP_011515631.1:p.Arg770Gly
XM_011517330.1:c.1369C>G	XP_011515632.1:p.Arg457Gly
XM_011517330.2:c.1369C>G	XP_011515632.1:p.Arg457Gly
XM_017013894.2:c.1540C>G	XP_016869383.1:p.Arg514Gly
XR_928355.2:n.3284C>G