Canonical Allele Identifier: CA1824603361

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360038G= , CM000670.2:g.140360038G=	GRCh38
NC_000008.10:g.141370137G= , CM000670.1:g.141370137G=	GRCh37
NC_000008.9:g.141439319G=	NCBI36
NG_016478.2:g.103542C=
NG_016478.3:g.103542C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1495+12C= MANE Select	ENSP00000405060.3:n.1495+12C=
ENST00000648948.2:c.1495+12C=	ENSP00000498020.1:n.1495+12C=
ENST00000389328.8:c.1789+12C=	ENSP00000373979.4:n.1789+12C=
ENST00000438773.2:c.1495+12C=	ENSP00000405060.2:n.1495+12C=
ENST00000520857.5:c.1025+12C=
NM_001160372.2:c.1495+12C=	NP_001153844.1:n.1495+12C=
NM_031466.6:c.1789+12C=	NP_113654.4:n.1789+12C=
XM_005251077.3:c.1495+12C=	XP_005251134.1:n.1495+12C=
XM_011517326.1:c.1762+12C=	XP_011515628.1:n.1762+12C=
XM_011517327.1:c.1789+12C=	XP_011515629.1:n.1789+12C=
XM_011517328.1:c.1789+12C=	XP_011515630.1:n.1789+12C=
XM_011517329.1:c.883+12C=	XP_011515631.1:n.883+12C=
XR_928355.1:n.1804+12C=
NM_001160372.3:c.1495+12C=	NP_001153844.1:n.1495+12C=
NM_001321646.1:c.1468+12C=	NP_001308575.1:n.1468+12C=
NM_031466.7:c.1789+12C=	NP_113654.4:n.1789+12C=
XM_011517326.2:c.1762+12C=	XP_011515628.1:n.1762+12C=
XM_011517328.2:c.1789+12C=	XP_011515630.1:n.1789+12C=
XM_017013893.1:c.1789+12C=	XP_016869382.1:n.1789+12C=
XM_017013894.2:c.115+12C=	XP_016869383.1:n.115+12C=
XR_928355.2:n.1804+12C=
NM_001160372.4:c.1495+12C= MANE Select	NP_001153844.1:n.1495+12C=
NM_001321646.2:c.1468+12C=	NP_001308575.1:n.1468+12C=
NM_001374682.1:c.1516+12C=	NP_001361611.1:n.1516+12C=
NM_001374683.1:c.1495+12C=	NP_001361612.1:n.1495+12C=
NM_001374684.1:c.1351+10926C=	NP_001361613.1:n.1351+10926C=
NM_031466.8:c.1495+12C=	NP_113654.5:n.1495+12C=
NR_164662.1:n.1584+12C=