Canonical Allele Identifier: CA187251431

Gene: TRAPPC9

Linked Data

• dbSNP Id: rs6992848
• MyVariant Identifiers: chr8:g.141150169T>G (hg19) ; chr8:g.140140070T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140140070T>G , CM000670.2:g.140140070T>G	GRCh38
NC_000008.10:g.141150169T>G , CM000670.1:g.141150169T>G	GRCh37
NC_000008.9:g.141219351T>G	NCBI36
NG_016478.2:g.323510A>C
NG_016478.3:g.323510A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000438773.4:c.2556+81389A>C MANE Select	ENSP00000405060.3:n.2556+81389A>C
ENST00000648948.2:c.2556+81389A>C	ENSP00000498020.1:n.2556+81389A>C
ENST00000389328.8:c.2850+81389A>C	ENSP00000373979.4:n.2850+81389A>C
ENST00000438773.2:c.2556+81389A>C	ENSP00000405060.2:n.2556+81389A>C
ENST00000517667.5:n.278+81389A>C
ENST00000520532.5:n.403+81389A>C
ENST00000520857.5:c.2086+81389A>C
ENST00000521667.5:n.961+81389A>C
NM_001160372.2:c.2556+81389A>C	NP_001153844.1:n.2556+81389A>C
NM_031466.6:c.2850+81389A>C	NP_113654.4:n.2850+81389A>C
XM_005251077.3:c.2556+81389A>C	XP_005251134.1:n.2556+81389A>C
XM_011517326.1:c.2823+81389A>C	XP_011515628.1:n.2823+81389A>C
XM_011517327.1:c.2850+81389A>C	XP_011515629.1:n.2850+81389A>C
XM_011517328.1:c.2850+81389A>C	XP_011515630.1:n.2850+81389A>C
XM_011517329.1:c.1944+81389A>C	XP_011515631.1:n.1944+81389A>C
XM_011517330.1:c.1005+81389A>C	XP_011515632.1:n.1005+81389A>C
XR_928355.1:n.2866-58027A>C
NM_001160372.3:c.2556+81389A>C	NP_001153844.1:n.2556+81389A>C
NM_001321646.1:c.2529+81389A>C	NP_001308575.1:n.2529+81389A>C
NM_031466.7:c.2850+81389A>C	NP_113654.4:n.2850+81389A>C
XM_011517326.2:c.2823+81389A>C	XP_011515628.1:n.2823+81389A>C
XM_011517328.2:c.2850+81389A>C	XP_011515630.1:n.2850+81389A>C
XM_011517330.2:c.1005+81389A>C	XP_011515632.1:n.1005+81389A>C
XM_017013894.2:c.1176+81389A>C	XP_016869383.1:n.1176+81389A>C
XR_928355.2:n.2866-58027A>C
NM_001160372.4:c.2556+81389A>C MANE Select	NP_001153844.1:n.2556+81389A>C
NM_001321646.2:c.2529+81389A>C	NP_001308575.1:n.2529+81389A>C
NM_001374682.1:c.2577+81389A>C	NP_001361611.1:n.2577+81389A>C
NM_001374683.1:c.2556+81389A>C	NP_001361612.1:n.2556+81389A>C
NM_001374684.1:c.2412+81389A>C	NP_001361613.1:n.2412+81389A>C
NM_031466.8:c.2556+81389A>C	NP_113654.5:n.2556+81389A>C
NR_164662.1:n.2645+81389A>C