Canonical Allele Identifier: CA2724930003
Gene: CNTN5 HGNC NCBI

Linked Data

dbSNP Id: rs2138902193

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.100302713_100302714insG , CM000673.2:g.100302713_100302714insG GRCh38
NC_000011.9:g.100173445_100173446insG , CM000673.1:g.100173445_100173446insG GRCh37
NC_000011.8:g.99678655_99678656insG NCBI36
NG_047156.1:g.1286738_1286739insG

Transcript Alleles

HGVS Amino-acid change
ENST00000524871.6:c.2620+3317_2620+3318insG MANE Select ENSP00000435637.1:n.2620+3317_2620+3318insG
ENST00000279463.7:c.2572+3317_2572+3318insG ENSP00000279463.4:n.2572+3317_2572+3318insG
ENST00000418526.6:c.2398+3317_2398+3318insG ENSP00000393229.2:n.2398+3317_2398+3318insG
ENST00000524560.1:n.868+3317_868+3318insG
ENST00000524871.5:c.2620+3317_2620+3318insG ENSP00000435637.1:n.2620+3317_2620+3318insG
ENST00000527185.5:c.2620+3317_2620+3318insG ENSP00000433575.1:n.2620+3317_2620+3318insG
ENST00000528682.5:c.2620+3317_2620+3318insG ENSP00000436185.1:n.2620+3317_2620+3318insG
ENST00000619298.1:c.2386+3317_2386+3318insG ENSP00000478120.1:n.2386+3317_2386+3318insG
NM_001243270.1:c.2620+3317_2620+3318insG NP_001230199.1:n.2620+3317_2620+3318insG
NM_001243271.1:c.2620+3317_2620+3318insG NP_001230200.1:n.2620+3317_2620+3318insG
NM_014361.3:c.2620+3317_2620+3318insG NP_055176.1:n.2620+3317_2620+3318insG
NM_175566.2:c.2398+3317_2398+3318insG NP_780775.1:n.2398+3317_2398+3318insG
XM_011542871.1:c.2398+3317_2398+3318insG XP_011541173.1:n.2398+3317_2398+3318insG
XM_017017926.1:c.2620+3317_2620+3318insG XP_016873415.1:n.2620+3317_2620+3318insG
XR_001747909.1:n.3003+3317_3003+3318insG
NM_014361.4:c.2620+3317_2620+3318insG MANE Select NP_055176.1:n.2620+3317_2620+3318insG
NM_001243270.2:c.2620+3317_2620+3318insG NP_001230199.1:n.2620+3317_2620+3318insG
NM_001243271.2:c.2620+3317_2620+3318insG NP_001230200.1:n.2620+3317_2620+3318insG