Canonical Allele Identifier: CA231560

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140291038C>T , CM000670.2:g.140291038C>T	GRCh38
NC_000008.10:g.141301137C>T , CM000670.1:g.141301137C>T	GRCh37
NC_000008.9:g.141370319C>T	NCBI36
NG_016478.2:g.172542G>A
NG_016478.3:g.172542G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1809G>A MANE Select	ENSP00000405060.3:p.Leu603=
ENST00000648948.2:c.1809G>A	ENSP00000498020.1:p.Leu603=
ENST00000389328.8:c.2103G>A	ENSP00000373979.4:p.Leu701=
ENST00000438773.2:c.1809G>A	ENSP00000405060.2:p.Leu603=
ENST00000520857.5:c.1339G>A
ENST00000521167.1:n.338G>A
ENST00000521667.5:n.214G>A
NM_001160372.2:c.1809G>A	NP_001153844.1:p.Leu603=
NM_031466.6:c.2103G>A	NP_113654.4:p.Leu701=
XM_005251077.3:c.1809G>A	XP_005251134.1:p.Leu603=
XM_011517326.1:c.2076G>A	XP_011515628.1:p.Leu692=
XM_011517327.1:c.2103G>A	XP_011515629.1:p.Leu701=
XM_011517328.1:c.2103G>A	XP_011515630.1:p.Leu701=
XM_011517329.1:c.1197G>A	XP_011515631.1:p.Leu399=
XM_011517330.1:c.258G>A	XP_011515632.1:p.Leu86=
XR_928355.1:n.2118G>A
NM_001160372.3:c.1809G>A	NP_001153844.1:p.Leu603=
NM_001321646.1:c.1782G>A	NP_001308575.1:p.Leu594=
NM_031466.7:c.2103G>A	NP_113654.4:p.Leu701=
XM_011517326.2:c.2076G>A	XP_011515628.1:p.Leu692=
XM_011517328.2:c.2103G>A	XP_011515630.1:p.Leu701=
XM_011517330.2:c.258G>A	XP_011515632.1:p.Leu86=
XM_017013893.1:c.2103G>A	XP_016869382.1:p.Leu701=
XM_017013894.2:c.429G>A	XP_016869383.1:p.Leu143=
XR_928355.2:n.2118G>A
NM_001160372.4:c.1809G>A MANE Select	NP_001153844.1:p.Leu603=
NM_001321646.2:c.1782G>A	NP_001308575.1:p.Leu594=
NM_001374682.1:c.1830G>A	NP_001361611.1:p.Leu610=
NM_001374683.1:c.1809G>A	NP_001361612.1:p.Leu603=
NM_001374684.1:c.1665G>A	NP_001361613.1:p.Leu555=
NM_031466.8:c.1809G>A	NP_113654.5:p.Leu603=
NR_164662.1:n.1898G>A