Canonical Allele Identifier: CA1750805166

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147491495T= , CM000669.2:g.147491495T=	GRCh38
NC_000007.13:g.147188587T= , CM000669.1:g.147188587T=	GRCh37
NC_000007.12:g.146819520T=	NCBI36
NG_007092.2:g.1380135T=
NG_007092.3:g.1380495T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1777+5454T= MANE Select	ENSP00000354778.3:n.1777+5454T=
ENST00000636870.1:n.1639+5454T=
ENST00000637694.1:n.1681-5126T=
ENST00000637825.1:n.1260+5454T=
ENST00000638117.1:n.1680+5454T=
ENST00000361727.7:c.1777+5454T=	ENSP00000354778.3:n.1777+5454T=
NM_014141.5:c.1777+5454T=	NP_054860.1:n.1777+5454T=
XM_006715919.1:c.265+5454T=	XP_006715982.1:n.265+5454T=
XM_017011950.2:c.1777+5454T=	XP_016867439.1:n.1777+5454T=
NM_014141.6:c.1777+5454T= MANE Select	NP_054860.1:n.1777+5454T=