Canonical Allele Identifier: CA4893747

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140451004T>C , CM000670.2:g.140451004T>C	GRCh38
NC_000008.10:g.141461103T>C , CM000670.1:g.141461103T>C	GRCh37
NC_000008.9:g.141530285T>C	NCBI36
NG_016478.2:g.12576A>G
NG_016478.3:g.12576A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.370A>G MANE Select	ENSP00000405060.3:p.Ile124Val
ENST00000648948.2:c.370A>G	ENSP00000498020.1:p.Ile124Val
ENST00000389328.8:c.664A>G	ENSP00000373979.4:p.Ile222Val
ENST00000438773.2:c.370A>G	ENSP00000405060.2:p.Ile124Val
NM_001160372.2:c.370A>G	NP_001153844.1:p.Ile124Val
NM_031466.6:c.664A>G	NP_113654.4:p.Ile222Val
XM_005251077.3:c.370A>G	XP_005251134.1:p.Ile124Val
XM_011517326.1:c.664A>G	XP_011515628.1:p.Ile222Val
XM_011517327.1:c.664A>G	XP_011515629.1:p.Ile222Val
XM_011517328.1:c.664A>G	XP_011515630.1:p.Ile222Val
XR_928355.1:n.679A>G
NM_001160372.3:c.370A>G	NP_001153844.1:p.Ile124Val
NM_001321646.1:c.370A>G	NP_001308575.1:p.Ile124Val
NM_031466.7:c.664A>G	NP_113654.4:p.Ile222Val
XM_011517326.2:c.664A>G	XP_011515628.1:p.Ile222Val
XM_011517328.2:c.664A>G	XP_011515630.1:p.Ile222Val
XM_017013893.1:c.664A>G	XP_016869382.1:p.Ile222Val
XR_928355.2:n.679A>G
NM_001160372.4:c.370A>G MANE Select	NP_001153844.1:p.Ile124Val
NM_001321646.2:c.370A>G	NP_001308575.1:p.Ile124Val
NM_001374682.1:c.370A>G	NP_001361611.1:p.Ile124Val
NM_001374683.1:c.370A>G	NP_001361612.1:p.Ile124Val
NM_001374684.1:c.370A>G	NP_001361613.1:p.Ile124Val
NM_031466.8:c.370A>G	NP_113654.5:p.Ile124Val
NR_164662.1:n.486A>G