Canonical Allele Identifier: CA2724929955

Gene: CNTN5

Linked Data

• dbSNP Id: rs2138902133

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.100302705_100302706insT , CM000673.2:g.100302705_100302706insT	GRCh38
NC_000011.9:g.100173437_100173438insT , CM000673.1:g.100173437_100173438insT	GRCh37
NC_000011.8:g.99678647_99678648insT	NCBI36
NG_047156.1:g.1286730_1286731insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000524871.6:c.2620+3309_2620+3310insT MANE Select	ENSP00000435637.1:n.2620+3309_2620+3310in...
ENST00000279463.7:c.2572+3309_2572+3310insT	ENSP00000279463.4:n.2572+3309_2572+3310in...
ENST00000418526.6:c.2398+3309_2398+3310insT	ENSP00000393229.2:n.2398+3309_2398+3310in...
ENST00000524560.1:n.868+3309_868+3310insT
ENST00000524871.5:c.2620+3309_2620+3310insT	ENSP00000435637.1:n.2620+3309_2620+3310in...
ENST00000527185.5:c.2620+3309_2620+3310insT	ENSP00000433575.1:n.2620+3309_2620+3310in...
ENST00000528682.5:c.2620+3309_2620+3310insT	ENSP00000436185.1:n.2620+3309_2620+3310in...
ENST00000619298.1:c.2386+3309_2386+3310insT	ENSP00000478120.1:n.2386+3309_2386+3310in...
NM_001243270.1:c.2620+3309_2620+3310insT	NP_001230199.1:n.2620+3309_2620+3310insT
NM_001243271.1:c.2620+3309_2620+3310insT	NP_001230200.1:n.2620+3309_2620+3310insT
NM_014361.3:c.2620+3309_2620+3310insT	NP_055176.1:n.2620+3309_2620+3310insT
NM_175566.2:c.2398+3309_2398+3310insT	NP_780775.1:n.2398+3309_2398+3310insT
XM_011542871.1:c.2398+3309_2398+3310insT	XP_011541173.1:n.2398+3309_2398+3310insT
XM_017017926.1:c.2620+3309_2620+3310insT	XP_016873415.1:n.2620+3309_2620+3310insT
XR_001747909.1:n.3003+3309_3003+3310insT
NM_014361.4:c.2620+3309_2620+3310insT MANE Select	NP_055176.1:n.2620+3309_2620+3310insT
NM_001243270.2:c.2620+3309_2620+3310insT	NP_001230199.1:n.2620+3309_2620+3310insT
NM_001243271.2:c.2620+3309_2620+3310insT	NP_001230200.1:n.2620+3309_2620+3310insT