Canonical Allele Identifier: CA12743714

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140287514T>C , CM000670.2:g.140287514T>C	GRCh38
NC_000008.10:g.141297613T>C , CM000670.1:g.141297613T>C	GRCh37
NC_000008.9:g.141366795T>C	NCBI36
NG_016478.2:g.176066A>G
NG_016478.3:g.176066A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1981+94A>G MANE Select	ENSP00000405060.3:n.1981+94A>G
ENST00000648948.2:c.1981+94A>G	ENSP00000498020.1:n.1981+94A>G
ENST00000389328.8:c.2275+94A>G	ENSP00000373979.4:n.2275+94A>G
ENST00000438773.2:c.1981+94A>G	ENSP00000405060.2:n.1981+94A>G
ENST00000520857.5:c.1511+94A>G
ENST00000521167.1:n.510+94A>G
ENST00000521667.5:n.386+94A>G
NM_001160372.2:c.1981+94A>G	NP_001153844.1:n.1981+94A>G
NM_031466.6:c.2275+94A>G	NP_113654.4:n.2275+94A>G
XM_005251077.3:c.1981+94A>G	XP_005251134.1:n.1981+94A>G
XM_011517326.1:c.2248+94A>G	XP_011515628.1:n.2248+94A>G
XM_011517327.1:c.2275+94A>G	XP_011515629.1:n.2275+94A>G
XM_011517328.1:c.2275+94A>G	XP_011515630.1:n.2275+94A>G
XM_011517329.1:c.1369+94A>G	XP_011515631.1:n.1369+94A>G
XM_011517330.1:c.430+94A>G	XP_011515632.1:n.430+94A>G
XR_928355.1:n.2290+94A>G
NM_001160372.3:c.1981+94A>G	NP_001153844.1:n.1981+94A>G
NM_001321646.1:c.1954+94A>G	NP_001308575.1:n.1954+94A>G
NM_031466.7:c.2275+94A>G	NP_113654.4:n.2275+94A>G
XM_011517326.2:c.2248+94A>G	XP_011515628.1:n.2248+94A>G
XM_011517328.2:c.2275+94A>G	XP_011515630.1:n.2275+94A>G
XM_011517330.2:c.430+94A>G	XP_011515632.1:n.430+94A>G
XM_017013893.1:c.2275+94A>G	XP_016869382.1:n.2275+94A>G
XM_017013894.2:c.601+94A>G	XP_016869383.1:n.601+94A>G
XR_928355.2:n.2290+94A>G
NM_001160372.4:c.1981+94A>G MANE Select	NP_001153844.1:n.1981+94A>G
NM_001321646.2:c.1954+94A>G	NP_001308575.1:n.1954+94A>G
NM_001374682.1:c.2002+94A>G	NP_001361611.1:n.2002+94A>G
NM_001374683.1:c.1981+94A>G	NP_001361612.1:n.1981+94A>G
NM_001374684.1:c.1837+94A>G	NP_001361613.1:n.1837+94A>G
NM_031466.8:c.1981+94A>G	NP_113654.5:n.1981+94A>G
NR_164662.1:n.2070+94A>G