Canonical Allele Identifier: CA652236801

Gene: CNTNAP2

Linked Data

• COSMIC: COSN25535946

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146778106dup , CM000669.2:g.146778106dup	GRCh38
NC_000007.13:g.146475198dup , CM000669.1:g.146475198dup	GRCh37
NC_000007.12:g.146106131dup	NCBI36
NG_007092.2:g.666746dup
NG_007092.3:g.667106dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.208+3725dup MANE Select	ENSP00000354778.3:n.208+3725dup
ENST00000636277.1:n.75+3725dup
ENST00000636561.1:n.111+3725dup
ENST00000636600.1:n.58+3725dup
ENST00000637150.1:n.137+3725dup
ENST00000637694.1:n.111+3725dup
ENST00000638117.1:n.111+3725dup
ENST00000361727.7:c.208+3725dup	ENSP00000354778.3:n.208+3725dup
ENST00000625365.2:c.208+3725dup	ENSP00000485955.1:n.208+3725dup
NM_014141.5:c.208+3725dup	NP_054860.1:n.208+3725dup
XM_017011950.2:c.208+3725dup	XP_016867439.1:n.208+3725dup
NM_014141.6:c.208+3725dup MANE Select	NP_054860.1:n.208+3725dup