Canonical Allele Identifier: CA372316653

Gene: TRAPPC9

Linked Data

• dbSNP Id: rs1194949731
• gnomAD v3: 8-140360185-T-C
• gnomAD v4: 8-140360185-T-C
• MyVariant Identifiers: chr8:g.141370284T>C (hg19) ; chr8:g.140360185T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360185T>C , CM000670.2:g.140360185T>C	GRCh38
NC_000008.10:g.141370284T>C , CM000670.1:g.141370284T>C	GRCh37
NC_000008.9:g.141439466T>C	NCBI36
NG_016478.2:g.103395A>G
NG_016478.3:g.103395A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1360A>G MANE Select	ENSP00000405060.3:p.Arg454Gly
ENST00000648948.2:c.1360A>G	ENSP00000498020.1:p.Arg454Gly
ENST00000389328.8:c.1654A>G	ENSP00000373979.4:p.Arg552Gly
ENST00000438773.2:c.1360A>G	ENSP00000405060.2:p.Arg454Gly
ENST00000520857.5:c.890A>G
NM_001160372.2:c.1360A>G	NP_001153844.1:p.Arg454Gly
NM_031466.6:c.1654A>G	NP_113654.4:p.Arg552Gly
XM_005251077.3:c.1360A>G	XP_005251134.1:p.Arg454Gly
XM_011517326.1:c.1627A>G	XP_011515628.1:p.Arg543Gly
XM_011517327.1:c.1654A>G	XP_011515629.1:p.Arg552Gly
XM_011517328.1:c.1654A>G	XP_011515630.1:p.Arg552Gly
XM_011517329.1:c.748A>G	XP_011515631.1:p.Arg250Gly
XR_928355.1:n.1669A>G
NM_001160372.3:c.1360A>G	NP_001153844.1:p.Arg454Gly
NM_001321646.1:c.1333A>G	NP_001308575.1:p.Arg445Gly
NM_031466.7:c.1654A>G	NP_113654.4:p.Arg552Gly
XM_011517326.2:c.1627A>G	XP_011515628.1:p.Arg543Gly
XM_011517328.2:c.1654A>G	XP_011515630.1:p.Arg552Gly
XM_017013893.1:c.1654A>G	XP_016869382.1:p.Arg552Gly
XM_017013894.2:c.-21A>G	XP_016869383.1:n.-21A>G
XR_928355.2:n.1669A>G
NM_001160372.4:c.1360A>G MANE Select	NP_001153844.1:p.Arg454Gly
NM_001321646.2:c.1333A>G	NP_001308575.1:p.Arg445Gly
NM_001374682.1:c.1381A>G	NP_001361611.1:p.Arg461Gly
NM_001374683.1:c.1360A>G	NP_001361612.1:p.Arg454Gly
NM_001374684.1:c.1351+10779A>G	NP_001361613.1:n.1351+10779A>G
NM_031466.8:c.1360A>G	NP_113654.5:p.Arg454Gly
NR_164662.1:n.1449A>G