Canonical Allele Identifier: CA13566265
Gene: CNTN5 HGNC NCBI

Linked Data

dbSNP Id: rs12282593

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.100000629A>G , CM000673.2:g.100000629A>G GRCh38
NC_000011.9:g.99871361A>G , CM000673.1:g.99871361A>G GRCh37
NC_000011.8:g.99376571A>G NCBI36
NG_047156.1:g.984654A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000524871.6:c.878-1405A>G MANE Select ENSP00000435637.1:n.878-1405A>G
ENST00000279463.7:c.830-1405A>G ENSP00000279463.4:n.830-1405A>G
ENST00000418526.6:c.656-1405A>G ENSP00000393229.2:n.656-1405A>G
ENST00000524871.5:c.878-1405A>G ENSP00000435637.1:n.878-1405A>G
ENST00000525236.1:n.205-1405A>G
ENST00000527185.5:c.878-1405A>G ENSP00000433575.1:n.878-1405A>G
ENST00000528682.5:c.878-1405A>G ENSP00000436185.1:n.878-1405A>G
ENST00000528727.5:n.1382-1405A>G
ENST00000619298.1:c.644-1405A>G ENSP00000478120.1:n.644-1405A>G
NM_001243270.1:c.878-1405A>G NP_001230199.1:n.878-1405A>G
NM_001243271.1:c.878-1405A>G NP_001230200.1:n.878-1405A>G
NM_014361.3:c.878-1405A>G NP_055176.1:n.878-1405A>G
NM_175566.2:c.656-1405A>G NP_780775.1:n.656-1405A>G
XM_011542871.1:c.656-1405A>G XP_011541173.1:n.656-1405A>G
XM_011542872.1:c.878-1405A>G XP_011541174.1:n.878-1405A>G
XM_011542873.1:c.878-1405A>G XP_011541175.1:n.878-1405A>G
XM_017017926.1:c.878-1405A>G XP_016873415.1:n.878-1405A>G
XM_017017927.1:c.878-1405A>G XP_016873416.1:n.878-1405A>G
XM_017017928.1:c.878-1405A>G XP_016873417.1:n.878-1405A>G
XM_017017929.1:c.656-1405A>G XP_016873418.1:n.656-1405A>G
XR_001747909.1:n.1382-1405A>G
NM_014361.4:c.878-1405A>G MANE Select NP_055176.1:n.878-1405A>G
NM_001243270.2:c.878-1405A>G NP_001230199.1:n.878-1405A>G
NM_001243271.2:c.878-1405A>G NP_001230200.1:n.878-1405A>G