Canonical Allele Identifier: CA15552944

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140275933G>A , CM000670.2:g.140275933G>A	GRCh38
NC_000008.10:g.141286032G>A , CM000670.1:g.141286032G>A	GRCh37
NC_000008.9:g.141355214G>A	NCBI36
NG_016478.2:g.187647C>T
NG_016478.3:g.187647C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.2115-112C>T MANE Select	ENSP00000405060.3:n.2115-112C>T
ENST00000648948.2:c.2115-112C>T	ENSP00000498020.1:n.2115-112C>T
ENST00000389328.8:c.2409-112C>T	ENSP00000373979.4:n.2409-112C>T
ENST00000438773.2:c.2115-112C>T	ENSP00000405060.2:n.2115-112C>T
ENST00000520857.5:c.1645-112C>T
ENST00000521667.5:n.520-112C>T
NM_001160372.2:c.2115-112C>T	NP_001153844.1:n.2115-112C>T
NM_031466.6:c.2409-112C>T	NP_113654.4:n.2409-112C>T
XM_005251077.3:c.2115-112C>T	XP_005251134.1:n.2115-112C>T
XM_011517326.1:c.2382-112C>T	XP_011515628.1:n.2382-112C>T
XM_011517327.1:c.2409-112C>T	XP_011515629.1:n.2409-112C>T
XM_011517328.1:c.2409-112C>T	XP_011515630.1:n.2409-112C>T
XM_011517329.1:c.1503-112C>T	XP_011515631.1:n.1503-112C>T
XM_011517330.1:c.564-112C>T	XP_011515632.1:n.564-112C>T
XR_928355.1:n.2424-112C>T
XR_928701.1:n.1231-5702G>A
XR_928702.1:n.1231-5702G>A
NM_001160372.3:c.2115-112C>T	NP_001153844.1:n.2115-112C>T
NM_001321646.1:c.2088-112C>T	NP_001308575.1:n.2088-112C>T
NM_031466.7:c.2409-112C>T	NP_113654.4:n.2409-112C>T
XM_011517326.2:c.2382-112C>T	XP_011515628.1:n.2382-112C>T
XM_011517328.2:c.2409-112C>T	XP_011515630.1:n.2409-112C>T
XM_011517330.2:c.564-112C>T	XP_011515632.1:n.564-112C>T
XM_017013893.1:c.2409-112C>T	XP_016869382.1:n.2409-112C>T
XM_017013894.2:c.735-112C>T	XP_016869383.1:n.735-112C>T
XR_001746116.1:n.2749-5702G>A
XR_001746117.1:n.2749-5702G>A
XR_928355.2:n.2424-112C>T
XR_928701.2:n.1170-5702G>A
NM_001160372.4:c.2115-112C>T MANE Select	NP_001153844.1:n.2115-112C>T
NM_001321646.2:c.2088-112C>T	NP_001308575.1:n.2088-112C>T
NM_001374682.1:c.2136-112C>T	NP_001361611.1:n.2136-112C>T
NM_001374683.1:c.2115-112C>T	NP_001361612.1:n.2115-112C>T
NM_001374684.1:c.1971-112C>T	NP_001361613.1:n.1971-112C>T
NM_031466.8:c.2115-112C>T	NP_113654.5:n.2115-112C>T
NR_164662.1:n.2204-112C>T