Canonical Allele Identifier: CA1995347177
Gene: CNTN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.100302832G= , CM000673.2:g.100302832G= GRCh38
NC_000011.9:g.100173564G= , CM000673.1:g.100173564G= GRCh37
NC_000011.8:g.99678774G= NCBI36
NG_047156.1:g.1286857G=

Transcript Alleles

HGVS Amino-acid change
ENST00000524871.6:c.2620+3436G= MANE Select ENSP00000435637.1:n.2620+3436G=
ENST00000279463.7:c.2572+3436G= ENSP00000279463.4:n.2572+3436G=
ENST00000418526.6:c.2398+3436G= ENSP00000393229.2:n.2398+3436G=
ENST00000524560.1:n.868+3436G=
ENST00000524871.5:c.2620+3436G= ENSP00000435637.1:n.2620+3436G=
ENST00000527185.5:c.2620+3436G= ENSP00000433575.1:n.2620+3436G=
ENST00000528682.5:c.2620+3436G= ENSP00000436185.1:n.2620+3436G=
ENST00000619298.1:c.2386+3436G= ENSP00000478120.1:n.2386+3436G=
NM_001243270.1:c.2620+3436G= NP_001230199.1:n.2620+3436G=
NM_001243271.1:c.2620+3436G= NP_001230200.1:n.2620+3436G=
NM_014361.3:c.2620+3436G= NP_055176.1:n.2620+3436G=
NM_175566.2:c.2398+3436G= NP_780775.1:n.2398+3436G=
XM_011542871.1:c.2398+3436G= XP_011541173.1:n.2398+3436G=
XM_017017926.1:c.2620+3436G= XP_016873415.1:n.2620+3436G=
XR_001747909.1:n.3003+3436G=
NM_014361.4:c.2620+3436G= MANE Select NP_055176.1:n.2620+3436G=
NM_001243270.2:c.2620+3436G= NP_001230199.1:n.2620+3436G=
NM_001243271.2:c.2620+3436G= NP_001230200.1:n.2620+3436G=