Canonical Allele Identifier: CA372316441

Gene: TRAPPC9

Linked Data

• MyVariant Identifiers: chr8:g.141370184A>T (hg19) ; chr8:g.140360085A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360085A>T , CM000670.2:g.140360085A>T	GRCh38
NC_000008.10:g.141370184A>T , CM000670.1:g.141370184A>T	GRCh37
NC_000008.9:g.141439366A>T	NCBI36
NG_016478.2:g.103495T>A
NG_016478.3:g.103495T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1460T>A MANE Select	ENSP00000405060.3:p.Leu487His
ENST00000648948.2:c.1460T>A	ENSP00000498020.1:p.Leu487His
ENST00000389328.8:c.1754T>A	ENSP00000373979.4:p.Leu585His
ENST00000438773.2:c.1460T>A	ENSP00000405060.2:p.Leu487His
ENST00000520857.5:c.990T>A
NM_001160372.2:c.1460T>A	NP_001153844.1:p.Leu487His
NM_031466.6:c.1754T>A	NP_113654.4:p.Leu585His
XM_005251077.3:c.1460T>A	XP_005251134.1:p.Leu487His
XM_011517326.1:c.1727T>A	XP_011515628.1:p.Leu576His
XM_011517327.1:c.1754T>A	XP_011515629.1:p.Leu585His
XM_011517328.1:c.1754T>A	XP_011515630.1:p.Leu585His
XM_011517329.1:c.848T>A	XP_011515631.1:p.Leu283His
XR_928355.1:n.1769T>A
NM_001160372.3:c.1460T>A	NP_001153844.1:p.Leu487His
NM_001321646.1:c.1433T>A	NP_001308575.1:p.Leu478His
NM_031466.7:c.1754T>A	NP_113654.4:p.Leu585His
XM_011517326.2:c.1727T>A	XP_011515628.1:p.Leu576His
XM_011517328.2:c.1754T>A	XP_011515630.1:p.Leu585His
XM_017013893.1:c.1754T>A	XP_016869382.1:p.Leu585His
XM_017013894.2:c.80T>A	XP_016869383.1:p.Leu27His
XR_928355.2:n.1769T>A
NM_001160372.4:c.1460T>A MANE Select	NP_001153844.1:p.Leu487His
NM_001321646.2:c.1433T>A	NP_001308575.1:p.Leu478His
NM_001374682.1:c.1481T>A	NP_001361611.1:p.Leu494His
NM_001374683.1:c.1460T>A	NP_001361612.1:p.Leu487His
NM_001374684.1:c.1351+10879T>A	NP_001361613.1:n.1351+10879T>A
NM_031466.8:c.1460T>A	NP_113654.5:p.Leu487His
NR_164662.1:n.1549T>A