Canonical Allele Identifier: CA463097201

Gene: TRAPPC9

Linked Data

• MyVariant Identifiers: chr8:g.141370225C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360126C>T , CM000670.2:g.140360126C>T	GRCh38
NC_000008.10:g.141370225C>T , CM000670.1:g.141370225C>T	GRCh37
NC_000008.9:g.141439407C>T	NCBI36
NG_016478.2:g.103454G>A
NG_016478.3:g.103454G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1419G>A MANE Select	ENSP00000405060.3:p.Arg473=
ENST00000648948.2:c.1419G>A	ENSP00000498020.1:p.Arg473=
ENST00000389328.8:c.1713G>A	ENSP00000373979.4:p.Arg571=
ENST00000438773.2:c.1419G>A	ENSP00000405060.2:p.Arg473=
ENST00000520857.5:c.949G>A
NM_001160372.2:c.1419G>A	NP_001153844.1:p.Arg473=
NM_031466.6:c.1713G>A	NP_113654.4:p.Arg571=
XM_005251077.3:c.1419G>A	XP_005251134.1:p.Arg473=
XM_011517326.1:c.1686G>A	XP_011515628.1:p.Arg562=
XM_011517327.1:c.1713G>A	XP_011515629.1:p.Arg571=
XM_011517328.1:c.1713G>A	XP_011515630.1:p.Arg571=
XM_011517329.1:c.807G>A	XP_011515631.1:p.Arg269=
XR_928355.1:n.1728G>A
NM_001160372.3:c.1419G>A	NP_001153844.1:p.Arg473=
NM_001321646.1:c.1392G>A	NP_001308575.1:p.Arg464=
NM_031466.7:c.1713G>A	NP_113654.4:p.Arg571=
XM_011517326.2:c.1686G>A	XP_011515628.1:p.Arg562=
XM_011517328.2:c.1713G>A	XP_011515630.1:p.Arg571=
XM_017013893.1:c.1713G>A	XP_016869382.1:p.Arg571=
XM_017013894.2:c.39G>A	XP_016869383.1:p.Arg13=
XR_928355.2:n.1728G>A
NM_001160372.4:c.1419G>A MANE Select	NP_001153844.1:p.Arg473=
NM_001321646.2:c.1392G>A	NP_001308575.1:p.Arg464=
NM_001374682.1:c.1440G>A	NP_001361611.1:p.Arg480=
NM_001374683.1:c.1419G>A	NP_001361612.1:p.Arg473=
NM_001374684.1:c.1351+10838G>A	NP_001361613.1:n.1351+10838G>A
NM_031466.8:c.1419G>A	NP_113654.5:p.Arg473=
NR_164662.1:n.1508G>A