Canonical Allele Identifier: CA585310397

Gene: TRAPPC9

Linked Data

• ClinVar Variation Id: 3007706
• ClinVar RCV Id: RCV003864305
• dbSNP Id: rs775482502
• gnomAD v2: 8-141370296-C-A
• gnomAD v3: 8-140360197-C-A
• gnomAD v4: 8-140360197-C-A
• MyVariant Identifiers: chr8:g.141370296C>A (hg19) ; chr8:g.140360197C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360197C>A , CM000670.2:g.140360197C>A	GRCh38
NC_000008.10:g.141370296C>A , CM000670.1:g.141370296C>A	GRCh37
NC_000008.9:g.141439478C>A	NCBI36
NG_016478.2:g.103383G>T
NG_016478.3:g.103383G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1352-4G>T MANE Select	ENSP00000405060.3:n.1352-4G>T
ENST00000648948.2:c.1352-4G>T	ENSP00000498020.1:n.1352-4G>T
ENST00000389328.8:c.1646-4G>T	ENSP00000373979.4:n.1646-4G>T
ENST00000438773.2:c.1352-4G>T	ENSP00000405060.2:n.1352-4G>T
ENST00000520857.5:c.882-4G>T
NM_001160372.2:c.1352-4G>T	NP_001153844.1:n.1352-4G>T
NM_031466.6:c.1646-4G>T	NP_113654.4:n.1646-4G>T
XM_005251077.3:c.1352-4G>T	XP_005251134.1:n.1352-4G>T
XM_011517326.1:c.1619-4G>T	XP_011515628.1:n.1619-4G>T
XM_011517327.1:c.1646-4G>T	XP_011515629.1:n.1646-4G>T
XM_011517328.1:c.1646-4G>T	XP_011515630.1:n.1646-4G>T
XM_011517329.1:c.740-4G>T	XP_011515631.1:n.740-4G>T
XR_928355.1:n.1661-4G>T
NM_001160372.3:c.1352-4G>T	NP_001153844.1:n.1352-4G>T
NM_001321646.1:c.1325-4G>T	NP_001308575.1:n.1325-4G>T
NM_031466.7:c.1646-4G>T	NP_113654.4:n.1646-4G>T
XM_011517326.2:c.1619-4G>T	XP_011515628.1:n.1619-4G>T
XM_011517328.2:c.1646-4G>T	XP_011515630.1:n.1646-4G>T
XM_017013893.1:c.1646-4G>T	XP_016869382.1:n.1646-4G>T
XM_017013894.2:c.-29-4G>T	XP_016869383.1:n.-29-4G>T
XR_928355.2:n.1661-4G>T
NM_001160372.4:c.1352-4G>T MANE Select	NP_001153844.1:n.1352-4G>T
NM_001321646.2:c.1325-4G>T	NP_001308575.1:n.1325-4G>T
NM_001374682.1:c.1373-4G>T	NP_001361611.1:n.1373-4G>T
NM_001374683.1:c.1352-4G>T	NP_001361612.1:n.1352-4G>T
NM_001374684.1:c.1351+10767G>T	NP_001361613.1:n.1351+10767G>T
NM_031466.8:c.1352-4G>T	NP_113654.5:n.1352-4G>T
NR_164662.1:n.1441-4G>T