Canonical Allele Identifier: CA4893634

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140435166G>A , CM000670.2:g.140435166G>A	GRCh38
NC_000008.10:g.141445265G>A , CM000670.1:g.141445265G>A	GRCh37
NC_000008.9:g.141514447G>A	NCBI36
NG_016478.2:g.28414C>T
NG_016478.3:g.28414C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.805C>T MANE Select	ENSP00000405060.3:p.Arg269Trp
ENST00000648948.2:c.805C>T	ENSP00000498020.1:p.Arg269Trp
ENST00000389328.8:c.1099C>T	ENSP00000373979.4:p.Arg367Trp
ENST00000438773.2:c.805C>T	ENSP00000405060.2:p.Arg269Trp
ENST00000520857.5:c.362C>T
ENST00000521944.1:n.32C>T
NM_001160372.2:c.805C>T	NP_001153844.1:p.Arg269Trp
NM_031466.6:c.1099C>T	NP_113654.4:p.Arg367Trp
XM_005251077.3:c.805C>T	XP_005251134.1:p.Arg269Trp
XM_011517326.1:c.1099C>T	XP_011515628.1:p.Arg367Trp
XM_011517327.1:c.1099C>T	XP_011515629.1:p.Arg367Trp
XM_011517328.1:c.1099C>T	XP_011515630.1:p.Arg367Trp
XM_011517329.1:c.193C>T	XP_011515631.1:p.Arg65Trp
XR_928355.1:n.1114C>T
NM_001160372.3:c.805C>T	NP_001153844.1:p.Arg269Trp
NM_001321646.1:c.805C>T	NP_001308575.1:p.Arg269Trp
NM_031466.7:c.1099C>T	NP_113654.4:p.Arg367Trp
XM_011517326.2:c.1099C>T	XP_011515628.1:p.Arg367Trp
XM_011517328.2:c.1099C>T	XP_011515630.1:p.Arg367Trp
XM_017013893.1:c.1099C>T	XP_016869382.1:p.Arg367Trp
XR_928355.2:n.1114C>T
NM_001160372.4:c.805C>T MANE Select	NP_001153844.1:p.Arg269Trp
NM_001321646.2:c.805C>T	NP_001308575.1:p.Arg269Trp
NM_001374682.1:c.826C>T	NP_001361611.1:p.Arg276Trp
NM_001374683.1:c.805C>T	NP_001361612.1:p.Arg269Trp
NM_001374684.1:c.805C>T	NP_001361613.1:p.Arg269Trp
NM_031466.8:c.805C>T	NP_113654.5:p.Arg269Trp
NR_164662.1:n.921C>T