Canonical Allele Identifier: CA1750436731

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146778383G= , CM000669.2:g.146778383G=	GRCh38
NC_000007.13:g.146475475G= , CM000669.1:g.146475475G=	GRCh37
NC_000007.12:g.146106408G=	NCBI36
NG_007092.2:g.667023G=
NG_007092.3:g.667383G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.208+4002G= MANE Select	ENSP00000354778.3:n.208+4002G=
ENST00000636277.1:n.75+4002G=
ENST00000636561.1:n.111+4002G=
ENST00000636600.1:n.59-3826G=
ENST00000637150.1:n.137+4002G=
ENST00000637694.1:n.111+4002G=
ENST00000638117.1:n.111+4002G=
ENST00000361727.7:c.208+4002G=	ENSP00000354778.3:n.208+4002G=
ENST00000625365.2:c.208+4002G=	ENSP00000485955.1:n.208+4002G=
NM_014141.5:c.208+4002G=	NP_054860.1:n.208+4002G=
XM_017011950.2:c.208+4002G=	XP_016867439.1:n.208+4002G=
NM_014141.6:c.208+4002G= MANE Select	NP_054860.1:n.208+4002G=