Canonical Allele Identifier: CA228113825

Gene: CNTN5

Linked Data

• dbSNP Id: rs373138365
• gnomAD v2: 11-100173564-G-A
• gnomAD v3: 11-100302832-G-A
• gnomAD v4: 11-100302832-G-A
• MyVariant Identifiers: chr11:g.100173564G>A (hg19) ; chr11:g.100302832G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.100302832G>A , CM000673.2:g.100302832G>A	GRCh38
NC_000011.9:g.100173564G>A , CM000673.1:g.100173564G>A	GRCh37
NC_000011.8:g.99678774G>A	NCBI36
NG_047156.1:g.1286857G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000524871.6:c.2620+3436G>A MANE Select	ENSP00000435637.1:n.2620+3436G>A
ENST00000279463.7:c.2572+3436G>A	ENSP00000279463.4:n.2572+3436G>A
ENST00000418526.6:c.2398+3436G>A	ENSP00000393229.2:n.2398+3436G>A
ENST00000524560.1:n.868+3436G>A
ENST00000524871.5:c.2620+3436G>A	ENSP00000435637.1:n.2620+3436G>A
ENST00000527185.5:c.2620+3436G>A	ENSP00000433575.1:n.2620+3436G>A
ENST00000528682.5:c.2620+3436G>A	ENSP00000436185.1:n.2620+3436G>A
ENST00000619298.1:c.2386+3436G>A	ENSP00000478120.1:n.2386+3436G>A
NM_001243270.1:c.2620+3436G>A	NP_001230199.1:n.2620+3436G>A
NM_001243271.1:c.2620+3436G>A	NP_001230200.1:n.2620+3436G>A
NM_014361.3:c.2620+3436G>A	NP_055176.1:n.2620+3436G>A
NM_175566.2:c.2398+3436G>A	NP_780775.1:n.2398+3436G>A
XM_011542871.1:c.2398+3436G>A	XP_011541173.1:n.2398+3436G>A
XM_017017926.1:c.2620+3436G>A	XP_016873415.1:n.2620+3436G>A
XR_001747909.1:n.3003+3436G>A
NM_014361.4:c.2620+3436G>A MANE Select	NP_055176.1:n.2620+3436G>A
NM_001243270.2:c.2620+3436G>A	NP_001230199.1:n.2620+3436G>A
NM_001243271.2:c.2620+3436G>A	NP_001230200.1:n.2620+3436G>A