Canonical Allele Identifier: CA4892735

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139731220C>T , CM000670.2:g.139731220C>T	GRCh38
NC_000008.10:g.140743463C>T , CM000670.1:g.140743463C>T	GRCh37
NC_000008.9:g.140812645C>T	NCBI36
NG_016478.2:g.732360G>A
NG_016478.3:g.732360G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.3288G>A MANE Select	ENSP00000405060.3:p.Pro1096=
ENST00000648948.2:c.3288G>A	ENSP00000498020.1:p.Pro1096=
ENST00000389328.8:c.3582G>A	ENSP00000373979.4:p.Pro1194=
ENST00000438773.2:c.3288G>A	ENSP00000405060.2:p.Pro1096=
ENST00000519482.1:n.375G>A
ENST00000520857.5:c.2818G>A
ENST00000521667.5:n.1693G>A
ENST00000521700.5:n.334G>A
ENST00000522504.5:n.441G>A
NM_001160372.2:c.3288G>A	NP_001153844.1:p.Pro1096=
NM_031466.6:c.3582G>A	NP_113654.4:p.Pro1194=
XM_005251077.3:c.3288G>A	XP_005251134.1:p.Pro1096=
XM_011517326.1:c.3555G>A	XP_011515628.1:p.Pro1185=
XM_011517329.1:c.2676G>A	XP_011515631.1:p.Pro892=
XM_011517330.1:c.1737G>A	XP_011515632.1:p.Pro579=
NM_001160372.3:c.3288G>A	NP_001153844.1:p.Pro1096=
NM_001321646.1:c.3261G>A	NP_001308575.1:p.Pro1087=
NM_031466.7:c.3582G>A	NP_113654.4:p.Pro1194=
XM_011517326.2:c.3555G>A	XP_011515628.1:p.Pro1185=
XM_011517330.2:c.1737G>A	XP_011515632.1:p.Pro579=
XM_017013894.2:c.1908G>A	XP_016869383.1:p.Pro636=
NM_001160372.4:c.3288G>A MANE Select	NP_001153844.1:p.Pro1096=
NM_001321646.2:c.3261G>A	NP_001308575.1:p.Pro1087=
NM_001374682.1:c.3309G>A	NP_001361611.1:p.Pro1103=
NM_001374683.1:c.3177G>A	NP_001361612.1:p.Pro1059=
NM_001374684.1:c.3144G>A	NP_001361613.1:p.Pro1048=
NM_031466.8:c.3288G>A	NP_113654.5:p.Pro1096=
NR_164662.1:n.3450G>A