Canonical Allele Identifier: CA682608658

Gene: CNTN5

Linked Data

• dbSNP Id: rs1359370035
• MyVariant Identifiers: chr11:g.99866190_99866193del (hg19) ; chr11:g.99995458_99995461del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.99995461_99995464del , CM000673.2:g.99995461_99995464del	GRCh38
NC_000011.9:g.99866193_99866196del , CM000673.1:g.99866193_99866196del	GRCh37
NC_000011.8:g.99371403_99371406del	NCBI36
NG_047156.1:g.979486_979489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524871.6:c.878-6573_878-6570del MANE Select	ENSP00000435637.1:n.878-6573_878-6570del
ENST00000279463.7:c.830-6573_830-6570del	ENSP00000279463.4:n.830-6573_830-6570del
ENST00000418526.6:c.656-6573_656-6570del	ENSP00000393229.2:n.656-6573_656-6570del
ENST00000524871.5:c.878-6573_878-6570del	ENSP00000435637.1:n.878-6573_878-6570del
ENST00000525236.1:n.205-6573_205-6570del
ENST00000527185.5:c.878-6573_878-6570del	ENSP00000433575.1:n.878-6573_878-6570del
ENST00000528682.5:c.878-6573_878-6570del	ENSP00000436185.1:n.878-6573_878-6570del
ENST00000528727.5:n.1382-6573_1382-6570del
ENST00000619298.1:c.644-6573_644-6570del	ENSP00000478120.1:n.644-6573_644-6570del
NM_001243270.1:c.878-6573_878-6570del	NP_001230199.1:n.878-6573_878-6570del
NM_001243271.1:c.878-6573_878-6570del	NP_001230200.1:n.878-6573_878-6570del
NM_014361.3:c.878-6573_878-6570del	NP_055176.1:n.878-6573_878-6570del
NM_175566.2:c.656-6573_656-6570del	NP_780775.1:n.656-6573_656-6570del
XM_011542871.1:c.656-6573_656-6570del	XP_011541173.1:n.656-6573_656-6570del
XM_011542872.1:c.878-6573_878-6570del	XP_011541174.1:n.878-6573_878-6570del
XM_011542873.1:c.878-6573_878-6570del	XP_011541175.1:n.878-6573_878-6570del
XM_017017926.1:c.878-6573_878-6570del	XP_016873415.1:n.878-6573_878-6570del
XM_017017927.1:c.878-6573_878-6570del	XP_016873416.1:n.878-6573_878-6570del
XM_017017928.1:c.878-6573_878-6570del	XP_016873417.1:n.878-6573_878-6570del
XM_017017929.1:c.656-6573_656-6570del	XP_016873418.1:n.656-6573_656-6570del
XR_001747909.1:n.1382-6573_1382-6570del
NM_014361.4:c.878-6573_878-6570del MANE Select	NP_055176.1:n.878-6573_878-6570del
NM_001243270.2:c.878-6573_878-6570del	NP_001230199.1:n.878-6573_878-6570del
NM_001243271.2:c.878-6573_878-6570del	NP_001230200.1:n.878-6573_878-6570del