Canonical Allele Identifier: CA372316406

Gene: TRAPPC9

Linked Data

• MyVariant Identifiers: chr8:g.141370169A>C (hg19) ; chr8:g.140360070A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360070A>C , CM000670.2:g.140360070A>C	GRCh38
NC_000008.10:g.141370169A>C , CM000670.1:g.141370169A>C	GRCh37
NC_000008.9:g.141439351A>C	NCBI36
NG_016478.2:g.103510T>G
NG_016478.3:g.103510T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1475T>G MANE Select	ENSP00000405060.3:p.Leu492Arg
ENST00000648948.2:c.1475T>G	ENSP00000498020.1:p.Leu492Arg
ENST00000389328.8:c.1769T>G	ENSP00000373979.4:p.Leu590Arg
ENST00000438773.2:c.1475T>G	ENSP00000405060.2:p.Leu492Arg
ENST00000520857.5:c.1005T>G
NM_001160372.2:c.1475T>G	NP_001153844.1:p.Leu492Arg
NM_031466.6:c.1769T>G	NP_113654.4:p.Leu590Arg
XM_005251077.3:c.1475T>G	XP_005251134.1:p.Leu492Arg
XM_011517326.1:c.1742T>G	XP_011515628.1:p.Leu581Arg
XM_011517327.1:c.1769T>G	XP_011515629.1:p.Leu590Arg
XM_011517328.1:c.1769T>G	XP_011515630.1:p.Leu590Arg
XM_011517329.1:c.863T>G	XP_011515631.1:p.Leu288Arg
XR_928355.1:n.1784T>G
NM_001160372.3:c.1475T>G	NP_001153844.1:p.Leu492Arg
NM_001321646.1:c.1448T>G	NP_001308575.1:p.Leu483Arg
NM_031466.7:c.1769T>G	NP_113654.4:p.Leu590Arg
XM_011517326.2:c.1742T>G	XP_011515628.1:p.Leu581Arg
XM_011517328.2:c.1769T>G	XP_011515630.1:p.Leu590Arg
XM_017013893.1:c.1769T>G	XP_016869382.1:p.Leu590Arg
XM_017013894.2:c.95T>G	XP_016869383.1:p.Leu32Arg
XR_928355.2:n.1784T>G
NM_001160372.4:c.1475T>G MANE Select	NP_001153844.1:p.Leu492Arg
NM_001321646.2:c.1448T>G	NP_001308575.1:p.Leu483Arg
NM_001374682.1:c.1496T>G	NP_001361611.1:p.Leu499Arg
NM_001374683.1:c.1475T>G	NP_001361612.1:p.Leu492Arg
NM_001374684.1:c.1351+10894T>G	NP_001361613.1:n.1351+10894T>G
NM_031466.8:c.1475T>G	NP_113654.5:p.Leu492Arg
NR_164662.1:n.1564T>G