Canonical Allele Identifier: CA2838554166

Gene: CNTN5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.99356203A>T , CM000673.2:g.99356203A>T	GRCh38
NC_000011.9:g.99226934A>T , CM000673.1:g.99226934A>T	GRCh37
NC_000011.8:g.98732144A>T	NCBI36
NG_047156.1:g.340228A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524871.6:c.-71+30719A>T MANE Select	ENSP00000435637.1:n.-71+30719A>T
ENST00000524871.5:c.-71+30719A>T	ENSP00000435637.1:n.-71+30719A>T
ENST00000527185.5:c.-71+30719A>T	ENSP00000433575.1:n.-71+30719A>T
ENST00000528682.5:c.-70-199942A>T	ENSP00000436185.1:n.-70-199942A>T
ENST00000528727.5:n.434+30719A>T
NM_001243270.1:c.-70-199942A>T	NP_001230199.1:n.-70-199942A>T
NM_001243271.1:c.-71+30719A>T	NP_001230200.1:n.-71+30719A>T
NM_014361.3:c.-71+30719A>T	NP_055176.1:n.-71+30719A>T
XM_011542871.1:c.-71+30719A>T	XP_011541173.1:n.-71+30719A>T
XM_011542872.1:c.-71+30719A>T	XP_011541174.1:n.-71+30719A>T
XM_011542873.1:c.-71+30719A>T	XP_011541175.1:n.-71+30719A>T
XM_017017926.1:c.-71+30719A>T	XP_016873415.1:n.-71+30719A>T
XM_017017927.1:c.-71+30719A>T	XP_016873416.1:n.-71+30719A>T
XM_017017928.1:c.-70-199942A>T	XP_016873417.1:n.-70-199942A>T
XM_017017929.1:c.-71+30719A>T	XP_016873418.1:n.-71+30719A>T
XR_001747909.1:n.434+30719A>T
NM_014361.4:c.-71+30719A>T MANE Select	NP_055176.1:n.-71+30719A>T
NM_001243270.2:c.-70-199942A>T	NP_001230199.1:n.-70-199942A>T
NM_001243271.2:c.-71+30719A>T	NP_001230200.1:n.-71+30719A>T