Canonical Allele Identifier: CA4892980

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139988740G>A , CM000670.2:g.139988740G>A	GRCh38
NC_000008.10:g.140998948G>A , CM000670.1:g.140998948G>A	GRCh37
NC_000008.9:g.141068130G>A	NCBI36
NG_016478.2:g.474840C>T
NG_016478.3:g.474840C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.2796C>T MANE Select	ENSP00000405060.3:p.Ala932=
ENST00000648948.2:c.2796C>T	ENSP00000498020.1:p.Ala932=
ENST00000389328.8:c.3090C>T	ENSP00000373979.4:p.Ala1030=
ENST00000438773.2:c.2796C>T	ENSP00000405060.2:p.Ala932=
ENST00000517667.5:n.518C>T
ENST00000520857.5:c.2326C>T
ENST00000521667.5:n.1201C>T
ENST00000523777.5:n.405C>T
ENST00000524162.5:n.222C>T
NM_001160372.2:c.2796C>T	NP_001153844.1:p.Ala932=
NM_031466.6:c.3090C>T	NP_113654.4:p.Ala1030=
XM_005251077.3:c.2796C>T	XP_005251134.1:p.Ala932=
XM_011517326.1:c.3063C>T	XP_011515628.1:p.Ala1021=
XM_011517327.1:c.3090C>T	XP_011515629.1:p.Ala1030=
XM_011517328.1:c.3090C>T	XP_011515630.1:p.Ala1030=
XM_011517329.1:c.2184C>T	XP_011515631.1:p.Ala728=
XM_011517330.1:c.1245C>T	XP_011515632.1:p.Ala415=
XR_928355.1:n.3160C>T
NM_001160372.3:c.2796C>T	NP_001153844.1:p.Ala932=
NM_001321646.1:c.2769C>T	NP_001308575.1:p.Ala923=
NM_031466.7:c.3090C>T	NP_113654.4:p.Ala1030=
XM_011517326.2:c.3063C>T	XP_011515628.1:p.Ala1021=
XM_011517328.2:c.3090C>T	XP_011515630.1:p.Ala1030=
XM_011517330.2:c.1245C>T	XP_011515632.1:p.Ala415=
XM_017013894.2:c.1416C>T	XP_016869383.1:p.Ala472=
XR_928355.2:n.3160C>T
NM_001160372.4:c.2796C>T MANE Select	NP_001153844.1:p.Ala932=
NM_001321646.2:c.2769C>T	NP_001308575.1:p.Ala923=
NM_001374682.1:c.2817C>T	NP_001361611.1:p.Ala939=
NM_001374683.1:c.2699+35197C>T	NP_001361612.1:n.2699+35197C>T
NM_001374684.1:c.2652C>T	NP_001361613.1:p.Ala884=
NM_031466.8:c.2796C>T	NP_113654.5:p.Ala932=
NR_164662.1:n.2885C>T