Canonical Allele Identifier: CA372316580

Gene: TRAPPC9

Linked Data

• MyVariant Identifiers: chr8:g.141370249A>T (hg19) ; chr8:g.140360150A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360150A>T , CM000670.2:g.140360150A>T	GRCh38
NC_000008.10:g.141370249A>T , CM000670.1:g.141370249A>T	GRCh37
NC_000008.9:g.141439431A>T	NCBI36
NG_016478.2:g.103430T>A
NG_016478.3:g.103430T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1395T>A MANE Select	ENSP00000405060.3:p.His465Gln
ENST00000648948.2:c.1395T>A	ENSP00000498020.1:p.His465Gln
ENST00000389328.8:c.1689T>A	ENSP00000373979.4:p.His563Gln
ENST00000438773.2:c.1395T>A	ENSP00000405060.2:p.His465Gln
ENST00000520857.5:c.925T>A
NM_001160372.2:c.1395T>A	NP_001153844.1:p.His465Gln
NM_031466.6:c.1689T>A	NP_113654.4:p.His563Gln
XM_005251077.3:c.1395T>A	XP_005251134.1:p.His465Gln
XM_011517326.1:c.1662T>A	XP_011515628.1:p.His554Gln
XM_011517327.1:c.1689T>A	XP_011515629.1:p.His563Gln
XM_011517328.1:c.1689T>A	XP_011515630.1:p.His563Gln
XM_011517329.1:c.783T>A	XP_011515631.1:p.His261Gln
XR_928355.1:n.1704T>A
NM_001160372.3:c.1395T>A	NP_001153844.1:p.His465Gln
NM_001321646.1:c.1368T>A	NP_001308575.1:p.His456Gln
NM_031466.7:c.1689T>A	NP_113654.4:p.His563Gln
XM_011517326.2:c.1662T>A	XP_011515628.1:p.His554Gln
XM_011517328.2:c.1689T>A	XP_011515630.1:p.His563Gln
XM_017013893.1:c.1689T>A	XP_016869382.1:p.His563Gln
XM_017013894.2:c.15T>A	XP_016869383.1:p.His5Gln
XR_928355.2:n.1704T>A
NM_001160372.4:c.1395T>A MANE Select	NP_001153844.1:p.His465Gln
NM_001321646.2:c.1368T>A	NP_001308575.1:p.His456Gln
NM_001374682.1:c.1416T>A	NP_001361611.1:p.His472Gln
NM_001374683.1:c.1395T>A	NP_001361612.1:p.His465Gln
NM_001374684.1:c.1351+10814T>A	NP_001361613.1:n.1351+10814T>A
NM_031466.8:c.1395T>A	NP_113654.5:p.His465Gln
NR_164662.1:n.1484T>A