Canonical Allele Identifier: CA144703

Gene: CNTN2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205059100del , CM000663.2:g.205059100del	GRCh38
NC_000001.10:g.205028228del , CM000663.1:g.205028228del	GRCh37
NC_000001.9:g.203294851del	NCBI36
NG_033845.1:g.20889del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331830.7:c.504del MANE Select	ENSP00000330633.4:p.Trp168CysfsTer?
ENST00000532366.2:c.*1091del	ENSP00000491665.1:n.*1091del
ENST00000636809.2:n.1423del
ENST00000638378.1:c.504del	ENSP00000492617.1:p.Trp168CysfsTer?
ENST00000638928.1:n.250del
ENST00000639015.1:n.754del
ENST00000639023.1:n.195del
ENST00000639302.1:c.504del	ENSP00000491671.1:p.Trp168CysfsTer?
ENST00000639971.1:c.504del	ENSP00000491959.1:p.Trp168CysfsTer?
ENST00000640326.1:c.504del	ENSP00000492495.1:p.Trp168CysfsTer?
ENST00000640352.1:c.*1302del	ENSP00000491080.1:n.*1302del
ENST00000640428.1:c.504del	ENSP00000491474.1:p.Trp168CysfsTer?
ENST00000331830.4:c.504del	ENSP00000330633.4:p.Trp168CysfsTer?
ENST00000481872.6:n.496del
ENST00000530117.5:n.298del
NM_005076.3:c.504del	NP_005067.1:p.Trp168CysfsTer?
XM_011509925.1:c.489del	XP_011508227.1:p.Trp163CysfsTer?
NM_001346083.1:c.504del	NP_001333012.1:p.Trp168CysfsTer?
NM_005076.4:c.504del	NP_005067.1:p.Trp168CysfsTer?
NR_144350.1:n.861del
XM_017002198.1:c.504del	XP_016857687.1:p.Trp168CysfsTer?
XM_017002199.2:c.489del	XP_016857688.1:p.Trp163CysfsTer?
XM_024449386.1:c.543del	XP_024305154.1:p.Trp181CysfsTer?
XM_024449387.1:c.177del	XP_024305155.1:p.Trp59CysfsTer?
XM_024449388.1:c.177del	XP_024305156.1:p.Trp59CysfsTer?
XM_024449389.1:c.543del	XP_024305157.1:p.Trp181CysfsTer?
NM_005076.5:c.504del MANE Select	NP_005067.1:p.Trp168CysfsTer?
NM_001346083.2:c.504del	NP_001333012.1:p.Trp168CysfsTer?
NR_144350.2:n.773del