Canonical Allele Identifier: CA4892798

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139732122G>A , CM000670.2:g.139732122G>A	GRCh38
NC_000008.10:g.140744365G>A , CM000670.1:g.140744365G>A	GRCh37
NC_000008.9:g.140813547G>A	NCBI36
NG_016478.2:g.731458C>T
NG_016478.3:g.731458C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.3136C>T MANE Select	ENSP00000405060.3:p.Arg1046Trp
ENST00000648948.2:c.3136C>T	ENSP00000498020.1:p.Arg1046Trp
ENST00000389328.8:c.3430C>T	ENSP00000373979.4:p.Arg1144Trp
ENST00000438773.2:c.3136C>T	ENSP00000405060.2:p.Arg1046Trp
ENST00000519482.1:n.223C>T
ENST00000520857.5:c.2666C>T
ENST00000521667.5:n.1541C>T
ENST00000521700.5:n.182C>T
ENST00000522504.5:n.289C>T
ENST00000524162.5:n.562C>T
NM_001160372.2:c.3136C>T	NP_001153844.1:p.Arg1046Trp
NM_031466.6:c.3430C>T	NP_113654.4:p.Arg1144Trp
XM_005251077.3:c.3136C>T	XP_005251134.1:p.Arg1046Trp
XM_011517326.1:c.3403C>T	XP_011515628.1:p.Arg1135Trp
XM_011517329.1:c.2524C>T	XP_011515631.1:p.Arg842Trp
XM_011517330.1:c.1585C>T	XP_011515632.1:p.Arg529Trp
NM_001160372.3:c.3136C>T	NP_001153844.1:p.Arg1046Trp
NM_001321646.1:c.3109C>T	NP_001308575.1:p.Arg1037Trp
NM_031466.7:c.3430C>T	NP_113654.4:p.Arg1144Trp
XM_011517326.2:c.3403C>T	XP_011515628.1:p.Arg1135Trp
XM_011517330.2:c.1585C>T	XP_011515632.1:p.Arg529Trp
XM_017013894.2:c.1756C>T	XP_016869383.1:p.Arg586Trp
NM_001160372.4:c.3136C>T MANE Select	NP_001153844.1:p.Arg1046Trp
NM_001321646.2:c.3109C>T	NP_001308575.1:p.Arg1037Trp
NM_001374682.1:c.3157C>T	NP_001361611.1:p.Arg1053Trp
NM_001374683.1:c.3025C>T	NP_001361612.1:p.Arg1009Trp
NM_001374684.1:c.2992C>T	NP_001361613.1:p.Arg998Trp
NM_031466.8:c.3136C>T	NP_113654.5:p.Arg1046Trp
NR_164662.1:n.3298C>T