Canonical Allele Identifier: CA4892712

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139731094A>T , CM000670.2:g.139731094A>T	GRCh38
NC_000008.10:g.140743337A>T , CM000670.1:g.140743337A>T	GRCh37
NC_000008.9:g.140812519A>T	NCBI36
NG_016478.2:g.732486T>A
NG_016478.3:g.732486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.3414T>A MANE Select	ENSP00000405060.3:p.Ser1138Arg
ENST00000648948.2:c.3414T>A	ENSP00000498020.1:p.Ser1138Arg
ENST00000389328.8:c.3708T>A	ENSP00000373979.4:p.Ser1236Arg
ENST00000438773.2:c.3414T>A	ENSP00000405060.2:p.Ser1138Arg
ENST00000519482.1:n.501T>A
ENST00000520857.5:c.2944T>A
ENST00000521667.5:n.1819T>A
ENST00000521700.5:n.460T>A
ENST00000522504.5:n.567T>A
NM_001160372.2:c.3414T>A	NP_001153844.1:p.Ser1138Arg
NM_031466.6:c.3708T>A	NP_113654.4:p.Ser1236Arg
XM_005251077.3:c.3414T>A	XP_005251134.1:p.Ser1138Arg
XM_011517326.1:c.3681T>A	XP_011515628.1:p.Ser1227Arg
XM_011517329.1:c.2802T>A	XP_011515631.1:p.Ser934Arg
XM_011517330.1:c.1863T>A	XP_011515632.1:p.Ser621Arg
NM_001160372.3:c.3414T>A	NP_001153844.1:p.Ser1138Arg
NM_001321646.1:c.3387T>A	NP_001308575.1:p.Ser1129Arg
NM_031466.7:c.3708T>A	NP_113654.4:p.Ser1236Arg
XM_011517326.2:c.3681T>A	XP_011515628.1:p.Ser1227Arg
XM_011517330.2:c.1863T>A	XP_011515632.1:p.Ser621Arg
XM_017013894.2:c.2034T>A	XP_016869383.1:p.Ser678Arg
NM_001160372.4:c.3414T>A MANE Select	NP_001153844.1:p.Ser1138Arg
NM_001321646.2:c.3387T>A	NP_001308575.1:p.Ser1129Arg
NM_001374682.1:c.3435T>A	NP_001361611.1:p.Ser1145Arg
NM_001374683.1:c.3303T>A	NP_001361612.1:p.Ser1101Arg
NM_001374684.1:c.3270T>A	NP_001361613.1:p.Ser1090Arg
NM_031466.8:c.3414T>A	NP_113654.5:p.Ser1138Arg
NR_164662.1:n.3576T>A