Canonical Allele Identifier: CA372316841

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140371005G>T , CM000670.2:g.140371005G>T	GRCh38
NC_000008.10:g.141381104G>T , CM000670.1:g.141381104G>T	GRCh37
NC_000008.9:g.141450286G>T	NCBI36
NG_016478.2:g.92575C>A
NG_016478.3:g.92575C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001160372.4:c.1310C>A MANE Select	NP_001153844.1:p.Pro437His
ENST00000438773.4:c.1310C>A MANE Select	ENSP00000405060.3:p.Pro437His
NM_001160372.2:c.1310C>A	NP_001153844.1:p.Pro437His
NM_001160372.3:c.1310C>A	NP_001153844.1:p.Pro437His
NM_001321646.1:c.1283C>A	NP_001308575.1:p.Pro428His
NM_001321646.2:c.1283C>A	NP_001308575.1:p.Pro428His
NM_001374682.1:c.1331C>A	NP_001361611.1:p.Pro444His
NM_001374683.1:c.1310C>A	NP_001361612.1:p.Pro437His
NM_001374684.1:c.1310C>A	NP_001361613.1:p.Pro437His
NM_031466.6:c.1604C>A	NP_113654.4:p.Pro535His
NM_031466.7:c.1604C>A	NP_113654.4:p.Pro535His
NM_031466.8:c.1310C>A	NP_113654.5:p.Pro437His
NR_164662.1:n.1399C>A
ENST00000389328.8:c.1604C>A	ENSP00000373979.4:p.Pro535His
ENST00000438773.2:c.1310C>A	ENSP00000405060.2:p.Pro437His
ENST00000520857.5:c.840C>A
ENST00000648948.2:c.1310C>A	ENSP00000498020.1:p.Pro437His
XM_005251077.3:c.1310C>A	XP_005251134.1:p.Pro437His
XM_011517326.1:c.1577C>A	XP_011515628.1:p.Pro526His
XM_011517326.2:c.1577C>A	XP_011515628.1:p.Pro526His
XM_011517327.1:c.1604C>A	XP_011515629.1:p.Pro535His
XM_011517328.1:c.1604C>A	XP_011515630.1:p.Pro535His
XM_011517328.2:c.1604C>A	XP_011515630.1:p.Pro535His
XM_011517329.1:c.698C>A	XP_011515631.1:p.Pro233His
XM_017013893.1:c.1604C>A	XP_016869382.1:p.Pro535His
XR_928355.1:n.1619C>A
XR_928355.2:n.1619C>A