Canonical Allele Identifier: CA372316591

Gene: TRAPPC9

Linked Data

• MyVariant Identifiers: chr8:g.141370254G>T (hg19) ; chr8:g.140360155G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360155G>T , CM000670.2:g.140360155G>T	GRCh38
NC_000008.10:g.141370254G>T , CM000670.1:g.141370254G>T	GRCh37
NC_000008.9:g.141439436G>T	NCBI36
NG_016478.2:g.103425C>A
NG_016478.3:g.103425C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1390C>A MANE Select	ENSP00000405060.3:p.Leu464Ile
ENST00000648948.2:c.1390C>A	ENSP00000498020.1:p.Leu464Ile
ENST00000389328.8:c.1684C>A	ENSP00000373979.4:p.Leu562Ile
ENST00000438773.2:c.1390C>A	ENSP00000405060.2:p.Leu464Ile
ENST00000520857.5:c.920C>A
NM_001160372.2:c.1390C>A	NP_001153844.1:p.Leu464Ile
NM_031466.6:c.1684C>A	NP_113654.4:p.Leu562Ile
XM_005251077.3:c.1390C>A	XP_005251134.1:p.Leu464Ile
XM_011517326.1:c.1657C>A	XP_011515628.1:p.Leu553Ile
XM_011517327.1:c.1684C>A	XP_011515629.1:p.Leu562Ile
XM_011517328.1:c.1684C>A	XP_011515630.1:p.Leu562Ile
XM_011517329.1:c.778C>A	XP_011515631.1:p.Leu260Ile
XR_928355.1:n.1699C>A
NM_001160372.3:c.1390C>A	NP_001153844.1:p.Leu464Ile
NM_001321646.1:c.1363C>A	NP_001308575.1:p.Leu455Ile
NM_031466.7:c.1684C>A	NP_113654.4:p.Leu562Ile
XM_011517326.2:c.1657C>A	XP_011515628.1:p.Leu553Ile
XM_011517328.2:c.1684C>A	XP_011515630.1:p.Leu562Ile
XM_017013893.1:c.1684C>A	XP_016869382.1:p.Leu562Ile
XM_017013894.2:c.10C>A	XP_016869383.1:p.Leu4Ile
XR_928355.2:n.1699C>A
NM_001160372.4:c.1390C>A MANE Select	NP_001153844.1:p.Leu464Ile
NM_001321646.2:c.1363C>A	NP_001308575.1:p.Leu455Ile
NM_001374682.1:c.1411C>A	NP_001361611.1:p.Leu471Ile
NM_001374683.1:c.1390C>A	NP_001361612.1:p.Leu464Ile
NM_001374684.1:c.1351+10809C>A	NP_001361613.1:n.1351+10809C>A
NM_031466.8:c.1390C>A	NP_113654.5:p.Leu464Ile
NR_164662.1:n.1479C>A