Canonical Allele Identifier: CA187199454

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139732352G>T , CM000670.2:g.139732352G>T	GRCh38
NC_000008.10:g.140744595G>T , CM000670.1:g.140744595G>T	GRCh37
NC_000008.9:g.140813777G>T	NCBI36
NG_016478.2:g.731228C>A
NG_016478.3:g.731228C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001160372.4:c.3056-150C>A MANE Select	NP_001153844.1:n.3056-150C>A
ENST00000438773.4:c.3056-150C>A MANE Select	ENSP00000405060.3:n.3056-150C>A
NM_001160372.2:c.3056-150C>A	NP_001153844.1:n.3056-150C>A
NM_001160372.3:c.3056-150C>A	NP_001153844.1:n.3056-150C>A
NM_001321646.1:c.3029-150C>A	NP_001308575.1:n.3029-150C>A
NM_001321646.2:c.3029-150C>A	NP_001308575.1:n.3029-150C>A
NM_001374682.1:c.3077-150C>A	NP_001361611.1:n.3077-150C>A
NM_001374683.1:c.2945-150C>A	NP_001361612.1:n.2945-150C>A
NM_001374684.1:c.2912-150C>A	NP_001361613.1:n.2912-150C>A
NM_031466.6:c.3350-150C>A	NP_113654.4:n.3350-150C>A
NM_031466.7:c.3350-150C>A	NP_113654.4:n.3350-150C>A
NM_031466.8:c.3056-150C>A	NP_113654.5:n.3056-150C>A
NR_164662.1:n.3218-150C>A
ENST00000389328.8:c.3350-150C>A	ENSP00000373979.4:n.3350-150C>A
ENST00000438773.2:c.3056-150C>A	ENSP00000405060.2:n.3056-150C>A
ENST00000519482.1:n.143-150C>A
ENST00000520857.5:c.2586-150C>A
ENST00000521667.5:n.1461-150C>A
ENST00000521700.5:n.102-150C>A
ENST00000522504.5:n.209-150C>A
ENST00000523777.5:n.665-150C>A
ENST00000524162.5:n.482-150C>A
ENST00000648948.2:c.3056-150C>A	ENSP00000498020.1:n.3056-150C>A
XM_005251077.3:c.3056-150C>A	XP_005251134.1:n.3056-150C>A
XM_011517326.1:c.3323-150C>A	XP_011515628.1:n.3323-150C>A
XM_011517326.2:c.3323-150C>A	XP_011515628.1:n.3323-150C>A
XM_011517329.1:c.2444-150C>A	XP_011515631.1:n.2444-150C>A
XM_011517330.1:c.1505-150C>A	XP_011515632.1:n.1505-150C>A
XM_011517330.2:c.1505-150C>A	XP_011515632.1:n.1505-150C>A
XM_017013894.2:c.1676-150C>A	XP_016869383.1:n.1676-150C>A
XR_928355.2:n.3420-150C>A