Canonical Allele Identifier: CA372316650

Gene: TRAPPC9

Linked Data

• MyVariant Identifiers: chr8:g.141370283C>G (hg19) ; chr8:g.140360184C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360184C>G , CM000670.2:g.140360184C>G	GRCh38
NC_000008.10:g.141370283C>G , CM000670.1:g.141370283C>G	GRCh37
NC_000008.9:g.141439465C>G	NCBI36
NG_016478.2:g.103396G>C
NG_016478.3:g.103396G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1361G>C MANE Select	ENSP00000405060.3:p.Arg454Thr
ENST00000648948.2:c.1361G>C	ENSP00000498020.1:p.Arg454Thr
ENST00000389328.8:c.1655G>C	ENSP00000373979.4:p.Arg552Thr
ENST00000438773.2:c.1361G>C	ENSP00000405060.2:p.Arg454Thr
ENST00000520857.5:c.891G>C
NM_001160372.2:c.1361G>C	NP_001153844.1:p.Arg454Thr
NM_031466.6:c.1655G>C	NP_113654.4:p.Arg552Thr
XM_005251077.3:c.1361G>C	XP_005251134.1:p.Arg454Thr
XM_011517326.1:c.1628G>C	XP_011515628.1:p.Arg543Thr
XM_011517327.1:c.1655G>C	XP_011515629.1:p.Arg552Thr
XM_011517328.1:c.1655G>C	XP_011515630.1:p.Arg552Thr
XM_011517329.1:c.749G>C	XP_011515631.1:p.Arg250Thr
XR_928355.1:n.1670G>C
NM_001160372.3:c.1361G>C	NP_001153844.1:p.Arg454Thr
NM_001321646.1:c.1334G>C	NP_001308575.1:p.Arg445Thr
NM_031466.7:c.1655G>C	NP_113654.4:p.Arg552Thr
XM_011517326.2:c.1628G>C	XP_011515628.1:p.Arg543Thr
XM_011517328.2:c.1655G>C	XP_011515630.1:p.Arg552Thr
XM_017013893.1:c.1655G>C	XP_016869382.1:p.Arg552Thr
XM_017013894.2:c.-20G>C	XP_016869383.1:n.-20G>C
XR_928355.2:n.1670G>C
NM_001160372.4:c.1361G>C MANE Select	NP_001153844.1:p.Arg454Thr
NM_001321646.2:c.1334G>C	NP_001308575.1:p.Arg445Thr
NM_001374682.1:c.1382G>C	NP_001361611.1:p.Arg461Thr
NM_001374683.1:c.1361G>C	NP_001361612.1:p.Arg454Thr
NM_001374684.1:c.1351+10780G>C	NP_001361613.1:n.1351+10780G>C
NM_031466.8:c.1361G>C	NP_113654.5:p.Arg454Thr
NR_164662.1:n.1450G>C