Canonical Allele Identifier: CA1995153385

Gene: CNTN5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.99994741_99994743delinsTTC , CM000673.2:g.99994741_99994743delinsTTC	GRCh38
NC_000011.9:g.99865473_99865475delinsTTC , CM000673.1:g.99865473_99865475delinsTTC	GRCh37
NC_000011.8:g.99370683_99370685delinsTTC	NCBI36
NG_047156.1:g.978766_978768delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524871.6:c.878-7293_878-7291delinsTTC MANE Select	ENSP00000435637.1:n.878-7293_878-7291delinsTTC
ENST00000279463.7:c.830-7293_830-7291delinsTTC	ENSP00000279463.4:n.830-7293_830-7291delinsTTC
ENST00000418526.6:c.656-7293_656-7291delinsTTC	ENSP00000393229.2:n.656-7293_656-7291delinsTTC
ENST00000524871.5:c.878-7293_878-7291delinsTTC	ENSP00000435637.1:n.878-7293_878-7291delinsTTC
ENST00000525236.1:n.205-7293_205-7291delinsTTC
ENST00000527185.5:c.878-7293_878-7291delinsTTC	ENSP00000433575.1:n.878-7293_878-7291delinsTTC
ENST00000528682.5:c.878-7293_878-7291delinsTTC	ENSP00000436185.1:n.878-7293_878-7291delinsTTC
ENST00000528727.5:n.1382-7293_1382-7291delinsTTC
ENST00000619298.1:c.644-7293_644-7291delinsTTC	ENSP00000478120.1:n.644-7293_644-7291delinsTTC
NM_001243270.1:c.878-7293_878-7291delinsTTC	NP_001230199.1:n.878-7293_878-7291delinsTTC
NM_001243271.1:c.878-7293_878-7291delinsTTC	NP_001230200.1:n.878-7293_878-7291delinsTTC
NM_014361.3:c.878-7293_878-7291delinsTTC	NP_055176.1:n.878-7293_878-7291delinsTTC
NM_175566.2:c.656-7293_656-7291delinsTTC	NP_780775.1:n.656-7293_656-7291delinsTTC
XM_011542871.1:c.656-7293_656-7291delinsTTC	XP_011541173.1:n.656-7293_656-7291delinsTTC
XM_011542872.1:c.878-7293_878-7291delinsTTC	XP_011541174.1:n.878-7293_878-7291delinsTTC
XM_011542873.1:c.878-7293_878-7291delinsTTC	XP_011541175.1:n.878-7293_878-7291delinsTTC
XM_017017926.1:c.878-7293_878-7291delinsTTC	XP_016873415.1:n.878-7293_878-7291delinsTTC
XM_017017927.1:c.878-7293_878-7291delinsTTC	XP_016873416.1:n.878-7293_878-7291delinsTTC
XM_017017928.1:c.878-7293_878-7291delinsTTC	XP_016873417.1:n.878-7293_878-7291delinsTTC
XM_017017929.1:c.656-7293_656-7291delinsTTC	XP_016873418.1:n.656-7293_656-7291delinsTTC
XR_001747909.1:n.1382-7293_1382-7291delinsTTC
NM_014361.4:c.878-7293_878-7291delinsTTC MANE Select	NP_055176.1:n.878-7293_878-7291delinsTTC
NM_001243270.2:c.878-7293_878-7291delinsTTC	NP_001230199.1:n.878-7293_878-7291delinsTTC
NM_001243271.2:c.878-7293_878-7291delinsTTC	NP_001230200.1:n.878-7293_878-7291delinsTTC