Canonical Allele Identifier: CA1750619970

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132956C= , CM000669.2:g.147132956C=	GRCh38
NC_000007.13:g.146830048C= , CM000669.1:g.146830048C=	GRCh37
NC_000007.12:g.146460981C=	NCBI36
NG_007092.2:g.1021596C=
NG_007092.3:g.1021956C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1348+447C= MANE Select	ENSP00000354778.3:n.1348+447C=
ENST00000636561.1:n.1251+447C=
ENST00000636870.1:n.1210+447C=
ENST00000637150.1:n.1277+447C=
ENST00000637694.1:n.1251+447C=
ENST00000637825.1:n.831+447C=
ENST00000638117.1:n.1251+447C=
ENST00000361727.7:c.1348+447C=	ENSP00000354778.3:n.1348+447C=
NM_014141.5:c.1348+447C=	NP_054860.1:n.1348+447C=
XM_017011950.2:c.1348+447C=	XP_016867439.1:n.1348+447C=
NM_014141.6:c.1348+447C= MANE Select	NP_054860.1:n.1348+447C=