Canonical Allele Identifier: CA1750805775

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147492687G= , CM000669.2:g.147492687G=	GRCh38
NC_000007.13:g.147189779G= , CM000669.1:g.147189779G=	GRCh37
NC_000007.12:g.146820712G=	NCBI36
NG_007092.2:g.1381327G=
NG_007092.3:g.1381687G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1777+6646G= MANE Select	ENSP00000354778.3:n.1777+6646G=
ENST00000636870.1:n.1639+6646G=
ENST00000637694.1:n.1681-3934G=
ENST00000637825.1:n.1260+6646G=
ENST00000638117.1:n.1680+6646G=
ENST00000361727.7:c.1777+6646G=	ENSP00000354778.3:n.1777+6646G=
NM_014141.5:c.1777+6646G=	NP_054860.1:n.1777+6646G=
XM_006715919.1:c.265+6646G=	XP_006715982.1:n.265+6646G=
XM_017011950.2:c.1777+6646G=	XP_016867439.1:n.1777+6646G=
NM_014141.6:c.1777+6646G= MANE Select	NP_054860.1:n.1777+6646G=