Canonical Allele Identifier: CA372732365

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139731096T>G , CM000670.2:g.139731096T>G	GRCh38
NC_000008.10:g.140743339T>G , CM000670.1:g.140743339T>G	GRCh37
NC_000008.9:g.140812521T>G	NCBI36
NG_016478.2:g.732484A>C
NG_016478.3:g.732484A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.3412A>C MANE Select	ENSP00000405060.3:p.Ser1138Arg
ENST00000648948.2:c.3412A>C	ENSP00000498020.1:p.Ser1138Arg
ENST00000389328.8:c.3706A>C	ENSP00000373979.4:p.Ser1236Arg
ENST00000438773.2:c.3412A>C	ENSP00000405060.2:p.Ser1138Arg
ENST00000519482.1:n.499A>C
ENST00000520857.5:c.2942A>C
ENST00000521667.5:n.1817A>C
ENST00000521700.5:n.458A>C
ENST00000522504.5:n.565A>C
NM_001160372.2:c.3412A>C	NP_001153844.1:p.Ser1138Arg
NM_031466.6:c.3706A>C	NP_113654.4:p.Ser1236Arg
XM_005251077.3:c.3412A>C	XP_005251134.1:p.Ser1138Arg
XM_011517326.1:c.3679A>C	XP_011515628.1:p.Ser1227Arg
XM_011517329.1:c.2800A>C	XP_011515631.1:p.Ser934Arg
XM_011517330.1:c.1861A>C	XP_011515632.1:p.Ser621Arg
NM_001160372.3:c.3412A>C	NP_001153844.1:p.Ser1138Arg
NM_001321646.1:c.3385A>C	NP_001308575.1:p.Ser1129Arg
NM_031466.7:c.3706A>C	NP_113654.4:p.Ser1236Arg
XM_011517326.2:c.3679A>C	XP_011515628.1:p.Ser1227Arg
XM_011517330.2:c.1861A>C	XP_011515632.1:p.Ser621Arg
XM_017013894.2:c.2032A>C	XP_016869383.1:p.Ser678Arg
NM_001160372.4:c.3412A>C MANE Select	NP_001153844.1:p.Ser1138Arg
NM_001321646.2:c.3385A>C	NP_001308575.1:p.Ser1129Arg
NM_001374682.1:c.3433A>C	NP_001361611.1:p.Ser1145Arg
NM_001374683.1:c.3301A>C	NP_001361612.1:p.Ser1101Arg
NM_001374684.1:c.3268A>C	NP_001361613.1:p.Ser1090Arg
NM_031466.8:c.3412A>C	NP_113654.5:p.Ser1138Arg
NR_164662.1:n.3574A>C