Canonical Allele Identifier: CA155775

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139988739C>T , CM000670.2:g.139988739C>T	GRCh38
NC_000008.10:g.140998947C>T , CM000670.1:g.140998947C>T	GRCh37
NC_000008.9:g.141068129C>T	NCBI36
NG_016478.2:g.474841G>A
NG_016478.3:g.474841G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.2797G>A MANE Select	ENSP00000405060.3:p.Gly933Ser
ENST00000648948.2:c.2797G>A	ENSP00000498020.1:p.Gly933Ser
ENST00000389328.8:c.3091G>A	ENSP00000373979.4:p.Gly1031Ser
ENST00000438773.2:c.2797G>A	ENSP00000405060.2:p.Gly933Ser
ENST00000520857.5:c.2327G>A
ENST00000521667.5:n.1202G>A
ENST00000523777.5:n.406G>A
ENST00000524162.5:n.223G>A
NM_001160372.2:c.2797G>A	NP_001153844.1:p.Gly933Ser
NM_031466.6:c.3091G>A	NP_113654.4:p.Gly1031Ser
XM_005251077.3:c.2797G>A	XP_005251134.1:p.Gly933Ser
XM_011517326.1:c.3064G>A	XP_011515628.1:p.Gly1022Ser
XM_011517327.1:c.3091G>A	XP_011515629.1:p.Gly1031Ser
XM_011517328.1:c.3091G>A	XP_011515630.1:p.Gly1031Ser
XM_011517329.1:c.2185G>A	XP_011515631.1:p.Gly729Ser
XM_011517330.1:c.1246G>A	XP_011515632.1:p.Gly416Ser
XR_928355.1:n.3161G>A
NM_001160372.3:c.2797G>A	NP_001153844.1:p.Gly933Ser
NM_001321646.1:c.2770G>A	NP_001308575.1:p.Gly924Ser
NM_031466.7:c.3091G>A	NP_113654.4:p.Gly1031Ser
XM_011517326.2:c.3064G>A	XP_011515628.1:p.Gly1022Ser
XM_011517328.2:c.3091G>A	XP_011515630.1:p.Gly1031Ser
XM_011517330.2:c.1246G>A	XP_011515632.1:p.Gly416Ser
XM_017013894.2:c.1417G>A	XP_016869383.1:p.Gly473Ser
XR_928355.2:n.3161G>A
NM_001160372.4:c.2797G>A MANE Select	NP_001153844.1:p.Gly933Ser
NM_001321646.2:c.2770G>A	NP_001308575.1:p.Gly924Ser
NM_001374682.1:c.2818G>A	NP_001361611.1:p.Gly940Ser
NM_001374683.1:c.2699+35198G>A	NP_001361612.1:n.2699+35198G>A
NM_001374684.1:c.2653G>A	NP_001361613.1:p.Gly885Ser
NM_031466.8:c.2797G>A	NP_113654.5:p.Gly933Ser
NR_164662.1:n.2886G>A