Canonical Allele Identifier: CA1750805729

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147492580A= , CM000669.2:g.147492580A=	GRCh38
NC_000007.13:g.147189672A= , CM000669.1:g.147189672A=	GRCh37
NC_000007.12:g.146820605A=	NCBI36
NG_007092.2:g.1381220A=
NG_007092.3:g.1381580A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1777+6539A= MANE Select	ENSP00000354778.3:n.1777+6539A=
ENST00000636870.1:n.1639+6539A=
ENST00000637694.1:n.1681-4041A=
ENST00000637825.1:n.1260+6539A=
ENST00000638117.1:n.1680+6539A=
ENST00000361727.7:c.1777+6539A=	ENSP00000354778.3:n.1777+6539A=
NM_014141.5:c.1777+6539A=	NP_054860.1:n.1777+6539A=
XM_006715919.1:c.265+6539A=	XP_006715982.1:n.265+6539A=
XM_017011950.2:c.1777+6539A=	XP_016867439.1:n.1777+6539A=
NM_014141.6:c.1777+6539A= MANE Select	NP_054860.1:n.1777+6539A=