Canonical Allele Identifier: CA208413

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139732083C>T , CM000670.2:g.139732083C>T	GRCh38
NC_000008.10:g.140744326C>T , CM000670.1:g.140744326C>T	GRCh37
NC_000008.9:g.140813508C>T	NCBI36
NG_016478.2:g.731497G>A
NG_016478.3:g.731497G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.3175G>A MANE Select	ENSP00000405060.3:p.Ala1059Thr
ENST00000648948.2:c.3175G>A	ENSP00000498020.1:p.Ala1059Thr
ENST00000389328.8:c.3469G>A	ENSP00000373979.4:p.Ala1157Thr
ENST00000438773.2:c.3175G>A	ENSP00000405060.2:p.Ala1059Thr
ENST00000519482.1:n.262G>A
ENST00000520857.5:c.2705G>A
ENST00000521667.5:n.1580G>A
ENST00000521700.5:n.221G>A
ENST00000522504.5:n.328G>A
NM_001160372.2:c.3175G>A	NP_001153844.1:p.Ala1059Thr
NM_031466.6:c.3469G>A	NP_113654.4:p.Ala1157Thr
XM_005251077.3:c.3175G>A	XP_005251134.1:p.Ala1059Thr
XM_011517326.1:c.3442G>A	XP_011515628.1:p.Ala1148Thr
XM_011517329.1:c.2563G>A	XP_011515631.1:p.Ala855Thr
XM_011517330.1:c.1624G>A	XP_011515632.1:p.Ala542Thr
NM_001160372.3:c.3175G>A	NP_001153844.1:p.Ala1059Thr
NM_001321646.1:c.3148G>A	NP_001308575.1:p.Ala1050Thr
NM_031466.7:c.3469G>A	NP_113654.4:p.Ala1157Thr
XM_011517326.2:c.3442G>A	XP_011515628.1:p.Ala1148Thr
XM_011517330.2:c.1624G>A	XP_011515632.1:p.Ala542Thr
XM_017013894.2:c.1795G>A	XP_016869383.1:p.Ala599Thr
NM_001160372.4:c.3175G>A MANE Select	NP_001153844.1:p.Ala1059Thr
NM_001321646.2:c.3148G>A	NP_001308575.1:p.Ala1050Thr
NM_001374682.1:c.3196G>A	NP_001361611.1:p.Ala1066Thr
NM_001374683.1:c.3064G>A	NP_001361612.1:p.Ala1022Thr
NM_001374684.1:c.3031G>A	NP_001361613.1:p.Ala1011Thr
NM_031466.8:c.3175G>A	NP_113654.5:p.Ala1059Thr
NR_164662.1:n.3337G>A