Canonical Allele Identifier: CA4892804

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139732141G>T , CM000670.2:g.139732141G>T	GRCh38
NC_000008.10:g.140744384G>T , CM000670.1:g.140744384G>T	GRCh37
NC_000008.9:g.140813566G>T	NCBI36
NG_016478.2:g.731439C>A
NG_016478.3:g.731439C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001160372.4:c.3117C>A MANE Select	NP_001153844.1:p.Asp1039Glu
ENST00000438773.4:c.3117C>A MANE Select	ENSP00000405060.3:p.Asp1039Glu
NM_001160372.2:c.3117C>A	NP_001153844.1:p.Asp1039Glu
NM_001160372.3:c.3117C>A	NP_001153844.1:p.Asp1039Glu
NM_001321646.1:c.3090C>A	NP_001308575.1:p.Asp1030Glu
NM_001321646.2:c.3090C>A	NP_001308575.1:p.Asp1030Glu
NM_001374682.1:c.3138C>A	NP_001361611.1:p.Asp1046Glu
NM_001374683.1:c.3006C>A	NP_001361612.1:p.Asp1002Glu
NM_001374684.1:c.2973C>A	NP_001361613.1:p.Asp991Glu
NM_031466.6:c.3411C>A	NP_113654.4:p.Asp1137Glu
NM_031466.7:c.3411C>A	NP_113654.4:p.Asp1137Glu
NM_031466.8:c.3117C>A	NP_113654.5:p.Asp1039Glu
NR_164662.1:n.3279C>A
ENST00000389328.8:c.3411C>A	ENSP00000373979.4:p.Asp1137Glu
ENST00000438773.2:c.3117C>A	ENSP00000405060.2:p.Asp1039Glu
ENST00000519482.1:n.204C>A
ENST00000520857.5:c.2647C>A
ENST00000521667.5:n.1522C>A
ENST00000521700.5:n.163C>A
ENST00000522504.5:n.270C>A
ENST00000524162.5:n.543C>A
ENST00000648948.2:c.3117C>A	ENSP00000498020.1:p.Asp1039Glu
XM_005251077.3:c.3117C>A	XP_005251134.1:p.Asp1039Glu
XM_011517326.1:c.3384C>A	XP_011515628.1:p.Asp1128Glu
XM_011517326.2:c.3384C>A	XP_011515628.1:p.Asp1128Glu
XM_011517329.1:c.2505C>A	XP_011515631.1:p.Asp835Glu
XM_011517330.1:c.1566C>A	XP_011515632.1:p.Asp522Glu
XM_011517330.2:c.1566C>A	XP_011515632.1:p.Asp522Glu
XM_017013894.2:c.1737C>A	XP_016869383.1:p.Asp579Glu