Canonical Allele Identifier: CA1994941657

Gene: CNTN5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.99622333C= , CM000673.2:g.99622333C=	GRCh38
NC_000011.9:g.99493064C= , CM000673.1:g.99493064C=	GRCh37
NC_000011.8:g.98998274C=	NCBI36
NG_047156.1:g.606358C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524871.6:c.55+66064C= MANE Select	ENSP00000435637.1:n.55+66064C=
ENST00000418526.6:c.55+66064C=	ENSP00000393229.2:n.55+66064C=
ENST00000524871.5:c.55+66064C=	ENSP00000435637.1:n.55+66064C=
ENST00000527185.5:c.55+66064C=	ENSP00000433575.1:n.55+66064C=
ENST00000528682.5:c.55+66064C=	ENSP00000436185.1:n.55+66064C=
ENST00000528727.5:n.559+66064C=
NM_001243270.1:c.55+66064C=	NP_001230199.1:n.55+66064C=
NM_001243271.1:c.55+66064C=	NP_001230200.1:n.55+66064C=
NM_014361.3:c.55+66064C=	NP_055176.1:n.55+66064C=
NM_175566.2:c.55+66064C=	NP_780775.1:n.55+66064C=
XM_011542871.1:c.55+66064C=	XP_011541173.1:n.55+66064C=
XM_011542872.1:c.55+66064C=	XP_011541174.1:n.55+66064C=
XM_011542873.1:c.55+66064C=	XP_011541175.1:n.55+66064C=
XM_017017926.1:c.55+66064C=	XP_016873415.1:n.55+66064C=
XM_017017927.1:c.55+66064C=	XP_016873416.1:n.55+66064C=
XM_017017928.1:c.55+66064C=	XP_016873417.1:n.55+66064C=
XM_017017929.1:c.55+66064C=	XP_016873418.1:n.55+66064C=
XR_001747909.1:n.559+66064C=
NM_014361.4:c.55+66064C= MANE Select	NP_055176.1:n.55+66064C=
NM_001243270.2:c.55+66064C=	NP_001230199.1:n.55+66064C=
NM_001243271.2:c.55+66064C=	NP_001230200.1:n.55+66064C=