Canonical Allele Identifier: CA1750805787

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147492705_147492707delinsTTC , CM000669.2:g.147492705_147492707delinsTTC	GRCh38
NC_000007.13:g.147189797_147189799delinsTTC , CM000669.1:g.147189797_147189799delinsTTC	GRCh37
NC_000007.12:g.146820730_146820732delinsTTC	NCBI36
NG_007092.2:g.1381345_1381347delinsTTC
NG_007092.3:g.1381705_1381707delinsTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1777+6664_1777+6666delinsTTC MANE Select	ENSP00000354778.3:n.1777+6664_1777+6666delinsTTC
ENST00000636870.1:n.1639+6664_1639+6666delinsTTC
ENST00000637694.1:n.1681-3916_1681-3914delinsTTC
ENST00000637825.1:n.1260+6664_1260+6666delinsTTC
ENST00000638117.1:n.1680+6664_1680+6666delinsTTC
ENST00000361727.7:c.1777+6664_1777+6666delinsTTC	ENSP00000354778.3:n.1777+6664_1777+6666delinsTTC
NM_014141.5:c.1777+6664_1777+6666delinsTTC	NP_054860.1:n.1777+6664_1777+6666delinsTTC
XM_006715919.1:c.265+6664_265+6666delinsTTC	XP_006715982.1:n.265+6664_265+6666delinsTTC
XM_017011950.2:c.1777+6664_1777+6666delinsTTC	XP_016867439.1:n.1777+6664_1777+6666delinsTTC
NM_014141.6:c.1777+6664_1777+6666delinsTTC MANE Select	NP_054860.1:n.1777+6664_1777+6666delinsTTC