Canonical Allele Identifier: CA13693381

Gene: PLXNC1 CEP83

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.94289428G>A , CM000674.2:g.94289428G>A	GRCh38
NC_000012.11:g.94683204G>A , CM000674.1:g.94683204G>A	GRCh37
NC_000012.10:g.93207335G>A	NCBI36
NG_050648.1:g.145706G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258526.9:c.3880-5058G>A (PLXNC1) MANE Select	ENSP00000258526.4:n.3880-5058G>A
ENST00000258526.8:c.3880-5058G>A (PLXNC1)	ENSP00000258526.4:n.3880-5058G>A
ENST00000545312.1:c.97-5058G>A (PLXNC1)	ENSP00000439225.1:n.97-5058G>A
ENST00000547057.5:c.1021-5058G>A (PLXNC1)	ENSP00000446720.1:n.1021-5058G>A
ENST00000549217.5:c.1003-5058G>A (PLXNC1)	ENSP00000446781.1:n.1003-5058G>A
NM_005761.2:c.3880-5058G>A (PLXNC1)	NP_005752.1:n.3880-5058G>A
NR_037687.1:n.673-5058G>A (PLXNC1)
XM_006719186.2:c.3841-5058G>A (PLXNC1)	XP_006719249.1:n.3841-5058G>A
XM_011537730.1:c.*1063G>A (PLXNC1)	XP_011536032.1:n.*1063G>A
XM_011538425.1:c.*31-18285C>T (CEP83)	XP_011536727.1:n.*31-18285C>T
XM_011538426.1:c.*30+19355C>T (CEP83)	XP_011536728.1:n.*30+19355C>T
XR_944471.1:n.3899-5058G>A (PLXNC1)
XR_944562.1:n.2664-6463C>T (CEP83)
XR_944563.1:n.2664-6463C>T (CEP83)
XR_944564.1:n.2664-6463C>T (CEP83)
XR_944565.1:n.2664-6463C>T (CEP83)
XR_944566.1:n.2664-7313C>T (CEP83)
XR_944567.1:n.2664-6463C>T (CEP83)
XR_944568.1:n.2664-6463C>T (CEP83)
XM_006719186.4:c.3841-5058G>A (PLXNC1)	XP_006719249.1:n.3841-5058G>A
XM_011537730.3:c.*1063G>A (PLXNC1)	XP_011536032.1:n.*1063G>A
XM_017018671.2:c.*1063G>A (PLXNC1)	XP_016874160.1:n.*1063G>A
XM_017018672.2:c.3880-5058G>A (PLXNC1)	XP_016874161.1:n.3880-5058G>A
XM_017019386.2:c.*31-3380C>T (CEP83)	XP_016874875.1:n.*31-3380C>T
XM_024449002.1:c.*31-18285C>T (CEP83)	XP_024304770.1:n.*31-18285C>T
XR_001748731.2:n.2686-6463C>T (CEP83)
XR_001748732.2:n.2686-6463C>T (CEP83)
XR_001748733.2:n.2686-7313C>T (CEP83)
XR_001748734.2:n.2686-6463C>T (CEP83)
XR_001748735.2:n.2686-6463C>T (CEP83)
XR_001748736.2:n.2686-6463C>T (CEP83)
NM_005761.3:c.3880-5058G>A (PLXNC1) MANE Select	NP_005752.1:n.3880-5058G>A
NR_037687.2:n.575-5058G>A (PLXNC1)