Canonical Allele Identifier: CA1995082040

Gene: CNTN5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.99886941_99886942delinsGA , CM000673.2:g.99886941_99886942delinsGA	GRCh38
NC_000011.9:g.99757673_99757674delinsGA , CM000673.1:g.99757673_99757674delinsGA	GRCh37
NC_000011.8:g.99262883_99262884delinsGA	NCBI36
NG_047156.1:g.870966_870967delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000524871.6:c.578-29113_578-29112delinsGA MANE Select	ENSP00000435637.1:n.578-29113_578-29112de...
ENST00000279463.7:c.530-29113_530-29112delinsGA	ENSP00000279463.4:n.530-29113_530-29112de...
ENST00000418526.6:c.356-29113_356-29112delinsGA	ENSP00000393229.2:n.356-29113_356-29112de...
ENST00000524871.5:c.578-29113_578-29112delinsGA	ENSP00000435637.1:n.578-29113_578-29112de...
ENST00000527185.5:c.578-29113_578-29112delinsGA	ENSP00000433575.1:n.578-29113_578-29112de...
ENST00000528682.5:c.578-29113_578-29112delinsGA	ENSP00000436185.1:n.578-29113_578-29112de...
ENST00000528727.5:n.1082-29113_1082-29112delinsGA
ENST00000619298.1:c.344-29113_344-29112delinsGA	ENSP00000478120.1:n.344-29113_344-29112de...
NM_001243270.1:c.578-29113_578-29112delinsGA	NP_001230199.1:n.578-29113_578-29112delin...
NM_001243271.1:c.578-29113_578-29112delinsGA	NP_001230200.1:n.578-29113_578-29112delin...
NM_014361.3:c.578-29113_578-29112delinsGA	NP_055176.1:n.578-29113_578-29112delinsGA...
NM_175566.2:c.356-29113_356-29112delinsGA	NP_780775.1:n.356-29113_356-29112delinsGA...
XM_011542871.1:c.356-29113_356-29112delinsGA	XP_011541173.1:n.356-29113_356-29112delin...
XM_011542872.1:c.578-29113_578-29112delinsGA	XP_011541174.1:n.578-29113_578-29112delin...
XM_011542873.1:c.578-29113_578-29112delinsGA	XP_011541175.1:n.578-29113_578-29112delin...
XM_017017926.1:c.578-29113_578-29112delinsGA	XP_016873415.1:n.578-29113_578-29112delin...
XM_017017927.1:c.578-29113_578-29112delinsGA	XP_016873416.1:n.578-29113_578-29112delin...
XM_017017928.1:c.578-29113_578-29112delinsGA	XP_016873417.1:n.578-29113_578-29112delin...
XM_017017929.1:c.356-29113_356-29112delinsGA	XP_016873418.1:n.356-29113_356-29112delin...
XR_001747909.1:n.1082-29113_1082-29112delinsGA
NM_014361.4:c.578-29113_578-29112delinsGA MANE Select	NP_055176.1:n.578-29113_578-29112delinsGA...
NM_001243270.2:c.578-29113_578-29112delinsGA	NP_001230199.1:n.578-29113_578-29112delin...
NM_001243271.2:c.578-29113_578-29112delinsGA	NP_001230200.1:n.578-29113_578-29112delin...