Canonical Allele Identifier: CA4893159

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140275691G>A , CM000670.2:g.140275691G>A	GRCh38
NC_000008.10:g.141285790G>A , CM000670.1:g.141285790G>A	GRCh37
NC_000008.9:g.141354972G>A	NCBI36
NG_016478.2:g.187889C>T
NG_016478.3:g.187889C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.2245C>T MANE Select	ENSP00000405060.3:p.Leu749=
ENST00000648948.2:c.2245C>T	ENSP00000498020.1:p.Leu749=
ENST00000389328.8:c.2539C>T	ENSP00000373979.4:p.Leu847=
ENST00000438773.2:c.2245C>T	ENSP00000405060.2:p.Leu749=
ENST00000520857.5:c.1775C>T
ENST00000521667.5:n.650C>T
ENST00000634178.1:c.63C>T
NM_001160372.2:c.2245C>T	NP_001153844.1:p.Leu749=
NM_031466.6:c.2539C>T	NP_113654.4:p.Leu847=
XM_005251077.3:c.2245C>T	XP_005251134.1:p.Leu749=
XM_011517326.1:c.2512C>T	XP_011515628.1:p.Leu838=
XM_011517327.1:c.2539C>T	XP_011515629.1:p.Leu847=
XM_011517328.1:c.2539C>T	XP_011515630.1:p.Leu847=
XM_011517329.1:c.1633C>T	XP_011515631.1:p.Leu545=
XM_011517330.1:c.694C>T	XP_011515632.1:p.Leu232=
XR_928355.1:n.2554C>T
XR_928701.1:n.1231-5944G>A
XR_928702.1:n.1231-5944G>A
NM_001160372.3:c.2245C>T	NP_001153844.1:p.Leu749=
NM_001321646.1:c.2218C>T	NP_001308575.1:p.Leu740=
NM_031466.7:c.2539C>T	NP_113654.4:p.Leu847=
XM_011517326.2:c.2512C>T	XP_011515628.1:p.Leu838=
XM_011517328.2:c.2539C>T	XP_011515630.1:p.Leu847=
XM_011517330.2:c.694C>T	XP_011515632.1:p.Leu232=
XM_017013893.1:c.2539C>T	XP_016869382.1:p.Leu847=
XM_017013894.2:c.865C>T	XP_016869383.1:p.Leu289=
XR_001746116.1:n.2749-5944G>A
XR_001746117.1:n.2749-5944G>A
XR_928355.2:n.2554C>T
XR_928701.2:n.1170-5944G>A
NM_001160372.4:c.2245C>T MANE Select	NP_001153844.1:p.Leu749=
NM_001321646.2:c.2218C>T	NP_001308575.1:p.Leu740=
NM_001374682.1:c.2266C>T	NP_001361611.1:p.Leu756=
NM_001374683.1:c.2245C>T	NP_001361612.1:p.Leu749=
NM_001374684.1:c.2101C>T	NP_001361613.1:p.Leu701=
NM_031466.8:c.2245C>T	NP_113654.5:p.Leu749=
NR_164662.1:n.2334C>T