Canonical Allele Identifier: CA2509093420

Gene: CNTN5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.99995081_99995082insATAAT , CM000673.2:g.99995081_99995082insATAAT	GRCh38
NC_000011.9:g.99865813_99865814insATAAT , CM000673.1:g.99865813_99865814insATAAT	GRCh37
NC_000011.8:g.99371023_99371024insATAAT	NCBI36
NG_047156.1:g.979106_979107insATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524871.6:c.878-6953_878-6952insATAAT MANE Select	ENSP00000435637.1:n.878-6953_878-6952insATAAT
ENST00000279463.7:c.830-6953_830-6952insATAAT	ENSP00000279463.4:n.830-6953_830-6952insATAAT
ENST00000418526.6:c.656-6953_656-6952insATAAT	ENSP00000393229.2:n.656-6953_656-6952insATAAT
ENST00000524871.5:c.878-6953_878-6952insATAAT	ENSP00000435637.1:n.878-6953_878-6952insATAAT
ENST00000525236.1:n.205-6953_205-6952insATAAT
ENST00000527185.5:c.878-6953_878-6952insATAAT	ENSP00000433575.1:n.878-6953_878-6952insATAAT
ENST00000528682.5:c.878-6953_878-6952insATAAT	ENSP00000436185.1:n.878-6953_878-6952insATAAT
ENST00000528727.5:n.1382-6953_1382-6952insATAAT
ENST00000619298.1:c.644-6953_644-6952insATAAT	ENSP00000478120.1:n.644-6953_644-6952insATAAT
NM_001243270.1:c.878-6953_878-6952insATAAT	NP_001230199.1:n.878-6953_878-6952insATAAT
NM_001243271.1:c.878-6953_878-6952insATAAT	NP_001230200.1:n.878-6953_878-6952insATAAT
NM_014361.3:c.878-6953_878-6952insATAAT	NP_055176.1:n.878-6953_878-6952insATAAT
NM_175566.2:c.656-6953_656-6952insATAAT	NP_780775.1:n.656-6953_656-6952insATAAT
XM_011542871.1:c.656-6953_656-6952insATAAT	XP_011541173.1:n.656-6953_656-6952insATAAT
XM_011542872.1:c.878-6953_878-6952insATAAT	XP_011541174.1:n.878-6953_878-6952insATAAT
XM_011542873.1:c.878-6953_878-6952insATAAT	XP_011541175.1:n.878-6953_878-6952insATAAT
XM_017017926.1:c.878-6953_878-6952insATAAT	XP_016873415.1:n.878-6953_878-6952insATAAT
XM_017017927.1:c.878-6953_878-6952insATAAT	XP_016873416.1:n.878-6953_878-6952insATAAT
XM_017017928.1:c.878-6953_878-6952insATAAT	XP_016873417.1:n.878-6953_878-6952insATAAT
XM_017017929.1:c.656-6953_656-6952insATAAT	XP_016873418.1:n.656-6953_656-6952insATAAT
XR_001747909.1:n.1382-6953_1382-6952insATAAT
NM_014361.4:c.878-6953_878-6952insATAAT MANE Select	NP_055176.1:n.878-6953_878-6952insATAAT
NM_001243270.2:c.878-6953_878-6952insATAAT	NP_001230199.1:n.878-6953_878-6952insATAAT
NM_001243271.2:c.878-6953_878-6952insATAAT	NP_001230200.1:n.878-6953_878-6952insATAAT