Canonical Allele Identifier: CA208932

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140287691G>A , CM000670.2:g.140287691G>A	GRCh38
NC_000008.10:g.141297790G>A , CM000670.1:g.141297790G>A	GRCh37
NC_000008.9:g.141366972G>A	NCBI36
NG_016478.2:g.175889C>T
NG_016478.3:g.175889C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1898C>T MANE Select	ENSP00000405060.3:p.Ala633Val
ENST00000648948.2:c.1898C>T	ENSP00000498020.1:p.Ala633Val
ENST00000389328.8:c.2192C>T	ENSP00000373979.4:p.Ala731Val
ENST00000438773.2:c.1898C>T	ENSP00000405060.2:p.Ala633Val
ENST00000520857.5:c.1428C>T
ENST00000521167.1:n.427C>T
ENST00000521667.5:n.303C>T
NM_001160372.2:c.1898C>T	NP_001153844.1:p.Ala633Val
NM_031466.6:c.2192C>T	NP_113654.4:p.Ala731Val
XM_005251077.3:c.1898C>T	XP_005251134.1:p.Ala633Val
XM_011517326.1:c.2165C>T	XP_011515628.1:p.Ala722Val
XM_011517327.1:c.2192C>T	XP_011515629.1:p.Ala731Val
XM_011517328.1:c.2192C>T	XP_011515630.1:p.Ala731Val
XM_011517329.1:c.1286C>T	XP_011515631.1:p.Ala429Val
XM_011517330.1:c.347C>T	XP_011515632.1:p.Ala116Val
XR_928355.1:n.2207C>T
NM_001160372.3:c.1898C>T	NP_001153844.1:p.Ala633Val
NM_001321646.1:c.1871C>T	NP_001308575.1:p.Ala624Val
NM_031466.7:c.2192C>T	NP_113654.4:p.Ala731Val
XM_011517326.2:c.2165C>T	XP_011515628.1:p.Ala722Val
XM_011517328.2:c.2192C>T	XP_011515630.1:p.Ala731Val
XM_011517330.2:c.347C>T	XP_011515632.1:p.Ala116Val
XM_017013893.1:c.2192C>T	XP_016869382.1:p.Ala731Val
XM_017013894.2:c.518C>T	XP_016869383.1:p.Ala173Val
XR_928355.2:n.2207C>T
NM_001160372.4:c.1898C>T MANE Select	NP_001153844.1:p.Ala633Val
NM_001321646.2:c.1871C>T	NP_001308575.1:p.Ala624Val
NM_001374682.1:c.1919C>T	NP_001361611.1:p.Ala640Val
NM_001374683.1:c.1898C>T	NP_001361612.1:p.Ala633Val
NM_001374684.1:c.1754C>T	NP_001361613.1:p.Ala585Val
NM_031466.8:c.1898C>T	NP_113654.5:p.Ala633Val
NR_164662.1:n.1987C>T