Canonical Allele Identifier: CA4893013

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140023983C>T , CM000670.2:g.140023983C>T	GRCh38
NC_000008.10:g.141034080C>T , CM000670.1:g.141034080C>T	GRCh37
NC_000008.9:g.141103262C>T	NCBI36
NG_016478.2:g.439597G>A
NG_016478.3:g.439597G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001160372.4:c.2653G>A MANE Select	NP_001153844.1:p.Glu885Lys
ENST00000438773.4:c.2653G>A MANE Select	ENSP00000405060.3:p.Glu885Lys
NM_001160372.2:c.2653G>A	NP_001153844.1:p.Glu885Lys
NM_001160372.3:c.2653G>A	NP_001153844.1:p.Glu885Lys
NM_001321646.1:c.2626G>A	NP_001308575.1:p.Glu876Lys
NM_001321646.2:c.2626G>A	NP_001308575.1:p.Glu876Lys
NM_001374682.1:c.2674G>A	NP_001361611.1:p.Glu892Lys
NM_001374683.1:c.2653G>A	NP_001361612.1:p.Glu885Lys
NM_001374684.1:c.2509G>A	NP_001361613.1:p.Glu837Lys
NM_031466.6:c.2947G>A	NP_113654.4:p.Glu983Lys
NM_031466.7:c.2947G>A	NP_113654.4:p.Glu983Lys
NM_031466.8:c.2653G>A	NP_113654.5:p.Glu885Lys
NR_164662.1:n.2742G>A
ENST00000389328.8:c.2947G>A	ENSP00000373979.4:p.Glu983Lys
ENST00000438773.2:c.2653G>A	ENSP00000405060.2:p.Glu885Lys
ENST00000517667.5:n.375G>A
ENST00000520532.5:n.500G>A
ENST00000520857.5:c.2183G>A
ENST00000521667.5:n.1058G>A
ENST00000523777.5:n.262G>A
ENST00000648948.2:c.2653G>A	ENSP00000498020.1:p.Glu885Lys
XM_005251077.3:c.2653G>A	XP_005251134.1:p.Glu885Lys
XM_011517326.1:c.2920G>A	XP_011515628.1:p.Glu974Lys
XM_011517326.2:c.2920G>A	XP_011515628.1:p.Glu974Lys
XM_011517327.1:c.2947G>A	XP_011515629.1:p.Glu983Lys
XM_011517328.1:c.2947G>A	XP_011515630.1:p.Glu983Lys
XM_011517328.2:c.2947G>A	XP_011515630.1:p.Glu983Lys
XM_011517329.1:c.2041G>A	XP_011515631.1:p.Glu681Lys
XM_011517330.1:c.1102G>A	XP_011515632.1:p.Glu368Lys
XM_011517330.2:c.1102G>A	XP_011515632.1:p.Glu368Lys
XM_017013894.2:c.1273G>A	XP_016869383.1:p.Glu425Lys
XR_928355.1:n.3017G>A
XR_928355.2:n.3017G>A