Canonical Allele Identifier: CA10627232

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139885946C>T , CM000670.2:g.139885946C>T	GRCh38
NC_000008.10:g.140898190C>T , CM000670.1:g.140898190C>T	GRCh37
NC_000008.9:g.140967372C>T	NCBI36
NG_016478.2:g.577634G>A
NG_016478.3:g.577634G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.2988G>A MANE Select	ENSP00000405060.3:p.Glu996=
ENST00000648948.2:c.2988G>A	ENSP00000498020.1:p.Glu996=
ENST00000389328.8:c.3282G>A	ENSP00000373979.4:p.Glu1094=
ENST00000438773.2:c.2988G>A	ENSP00000405060.2:p.Glu996=
ENST00000519482.1:n.142+22671G>A
ENST00000520857.5:c.2518G>A
ENST00000521667.5:n.1393G>A
ENST00000523777.5:n.597G>A
ENST00000524162.5:n.414G>A
NM_001160372.2:c.2988G>A	NP_001153844.1:p.Glu996=
NM_031466.6:c.3282G>A	NP_113654.4:p.Glu1094=
XM_005251077.3:c.2988G>A	XP_005251134.1:p.Glu996=
XM_011517326.1:c.3255G>A	XP_011515628.1:p.Glu1085=
XM_011517327.1:c.3282G>A	XP_011515629.1:p.Glu1094=
XM_011517328.1:c.3282G>A	XP_011515630.1:p.Glu1094=
XM_011517329.1:c.2376G>A	XP_011515631.1:p.Glu792=
XM_011517330.1:c.1437G>A	XP_011515632.1:p.Glu479=
NM_001160372.3:c.2988G>A	NP_001153844.1:p.Glu996=
NM_001321646.1:c.2961G>A	NP_001308575.1:p.Glu987=
NM_031466.7:c.3282G>A	NP_113654.4:p.Glu1094=
XM_011517326.2:c.3255G>A	XP_011515628.1:p.Glu1085=
XM_011517328.2:c.3282G>A	XP_011515630.1:p.Glu1094=
XM_011517330.2:c.1437G>A	XP_011515632.1:p.Glu479=
XM_017013894.2:c.1608G>A	XP_016869383.1:p.Glu536=
XR_928355.2:n.3352G>A
NM_001160372.4:c.2988G>A MANE Select	NP_001153844.1:p.Glu996=
NM_001321646.2:c.2961G>A	NP_001308575.1:p.Glu987=
NM_001374682.1:c.3009G>A	NP_001361611.1:p.Glu1003=
NM_001374683.1:c.2877G>A	NP_001361612.1:p.Glu959=
NM_001374684.1:c.2844G>A	NP_001361613.1:p.Glu948=
NM_031466.8:c.2988G>A	NP_113654.5:p.Glu996=
NR_164662.1:n.3077G>A