Canonical Allele Identifier: CA1750436667

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146778238A= , CM000669.2:g.146778238A=	GRCh38
NC_000007.13:g.146475330A= , CM000669.1:g.146475330A=	GRCh37
NC_000007.12:g.146106263A=	NCBI36
NG_007092.2:g.666878A=
NG_007092.3:g.667238A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.208+3857A= MANE Select	ENSP00000354778.3:n.208+3857A=
ENST00000636277.1:n.75+3857A=
ENST00000636561.1:n.111+3857A=
ENST00000636600.1:n.58+3857A=
ENST00000637150.1:n.137+3857A=
ENST00000637694.1:n.111+3857A=
ENST00000638117.1:n.111+3857A=
ENST00000361727.7:c.208+3857A=	ENSP00000354778.3:n.208+3857A=
ENST00000625365.2:c.208+3857A=	ENSP00000485955.1:n.208+3857A=
NM_014141.5:c.208+3857A=	NP_054860.1:n.208+3857A=
XM_017011950.2:c.208+3857A=	XP_016867439.1:n.208+3857A=
NM_014141.6:c.208+3857A= MANE Select	NP_054860.1:n.208+3857A=