Canonical Allele Identifier: CA4892790

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139732100C>T , CM000670.2:g.139732100C>T	GRCh38
NC_000008.10:g.140744343C>T , CM000670.1:g.140744343C>T	GRCh37
NC_000008.9:g.140813525C>T	NCBI36
NG_016478.2:g.731480G>A
NG_016478.3:g.731480G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001160372.4:c.3158G>A MANE Select	NP_001153844.1:p.Arg1053His
ENST00000438773.4:c.3158G>A MANE Select	ENSP00000405060.3:p.Arg1053His
NM_001160372.2:c.3158G>A	NP_001153844.1:p.Arg1053His
NM_001160372.3:c.3158G>A	NP_001153844.1:p.Arg1053His
NM_001321646.1:c.3131G>A	NP_001308575.1:p.Arg1044His
NM_001321646.2:c.3131G>A	NP_001308575.1:p.Arg1044His
NM_001374682.1:c.3179G>A	NP_001361611.1:p.Arg1060His
NM_001374683.1:c.3047G>A	NP_001361612.1:p.Arg1016His
NM_001374684.1:c.3014G>A	NP_001361613.1:p.Arg1005His
NM_031466.6:c.3452G>A	NP_113654.4:p.Arg1151His
NM_031466.7:c.3452G>A	NP_113654.4:p.Arg1151His
NM_031466.8:c.3158G>A	NP_113654.5:p.Arg1053His
NR_164662.1:n.3320G>A
ENST00000389328.8:c.3452G>A	ENSP00000373979.4:p.Arg1151His
ENST00000438773.2:c.3158G>A	ENSP00000405060.2:p.Arg1053His
ENST00000519482.1:n.245G>A
ENST00000520857.5:c.2688G>A
ENST00000521667.5:n.1563G>A
ENST00000521700.5:n.204G>A
ENST00000522504.5:n.311G>A
ENST00000524162.5:n.584G>A
ENST00000648948.2:c.3158G>A	ENSP00000498020.1:p.Arg1053His
XM_005251077.3:c.3158G>A	XP_005251134.1:p.Arg1053His
XM_011517326.1:c.3425G>A	XP_011515628.1:p.Arg1142His
XM_011517326.2:c.3425G>A	XP_011515628.1:p.Arg1142His
XM_011517329.1:c.2546G>A	XP_011515631.1:p.Arg849His
XM_011517330.1:c.1607G>A	XP_011515632.1:p.Arg536His
XM_011517330.2:c.1607G>A	XP_011515632.1:p.Arg536His
XM_017013894.2:c.1778G>A	XP_016869383.1:p.Arg593His