Canonical Allele Identifier: CA372316356

Gene: TRAPPC9

Linked Data

• MyVariant Identifiers: chr8:g.141370147A>G (hg19) ; chr8:g.140360048A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360048A>G , CM000670.2:g.140360048A>G	GRCh38
NC_000008.10:g.141370147A>G , CM000670.1:g.141370147A>G	GRCh37
NC_000008.9:g.141439329A>G	NCBI36
NG_016478.2:g.103532T>C
NG_016478.3:g.103532T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1495+2T>C MANE Select	ENSP00000405060.3:n.1495+2T>C
ENST00000648948.2:c.1495+2T>C	ENSP00000498020.1:n.1495+2T>C
ENST00000389328.8:c.1789+2T>C	ENSP00000373979.4:n.1789+2T>C
ENST00000438773.2:c.1495+2T>C	ENSP00000405060.2:n.1495+2T>C
ENST00000520857.5:c.1025+2T>C
NM_001160372.2:c.1495+2T>C	NP_001153844.1:n.1495+2T>C
NM_031466.6:c.1789+2T>C	NP_113654.4:n.1789+2T>C
XM_005251077.3:c.1495+2T>C	XP_005251134.1:n.1495+2T>C
XM_011517326.1:c.1762+2T>C	XP_011515628.1:n.1762+2T>C
XM_011517327.1:c.1789+2T>C	XP_011515629.1:n.1789+2T>C
XM_011517328.1:c.1789+2T>C	XP_011515630.1:n.1789+2T>C
XM_011517329.1:c.883+2T>C	XP_011515631.1:n.883+2T>C
XR_928355.1:n.1804+2T>C
NM_001160372.3:c.1495+2T>C	NP_001153844.1:n.1495+2T>C
NM_001321646.1:c.1468+2T>C	NP_001308575.1:n.1468+2T>C
NM_031466.7:c.1789+2T>C	NP_113654.4:n.1789+2T>C
XM_011517326.2:c.1762+2T>C	XP_011515628.1:n.1762+2T>C
XM_011517328.2:c.1789+2T>C	XP_011515630.1:n.1789+2T>C
XM_017013893.1:c.1789+2T>C	XP_016869382.1:n.1789+2T>C
XM_017013894.2:c.115+2T>C	XP_016869383.1:n.115+2T>C
XR_928355.2:n.1804+2T>C
NM_001160372.4:c.1495+2T>C MANE Select	NP_001153844.1:n.1495+2T>C
NM_001321646.2:c.1468+2T>C	NP_001308575.1:n.1468+2T>C
NM_001374682.1:c.1516+2T>C	NP_001361611.1:n.1516+2T>C
NM_001374683.1:c.1495+2T>C	NP_001361612.1:n.1495+2T>C
NM_001374684.1:c.1351+10916T>C	NP_001361613.1:n.1351+10916T>C
NM_031466.8:c.1495+2T>C	NP_113654.5:n.1495+2T>C
NR_164662.1:n.1584+2T>C