Canonical Allele Identifier: CA1750619978

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132988G= , CM000669.2:g.147132988G=	GRCh38
NC_000007.13:g.146830080G= , CM000669.1:g.146830080G=	GRCh37
NC_000007.12:g.146461013G=	NCBI36
NG_007092.2:g.1021628G=
NG_007092.3:g.1021988G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1348+479G= MANE Select	ENSP00000354778.3:n.1348+479G=
ENST00000636561.1:n.1251+479G=
ENST00000636870.1:n.1210+479G=
ENST00000637150.1:n.1277+479G=
ENST00000637694.1:n.1251+479G=
ENST00000637825.1:n.831+479G=
ENST00000638117.1:n.1251+479G=
ENST00000361727.7:c.1348+479G=	ENSP00000354778.3:n.1348+479G=
NM_014141.5:c.1348+479G=	NP_054860.1:n.1348+479G=
XM_017011950.2:c.1348+479G=	XP_016867439.1:n.1348+479G=
NM_014141.6:c.1348+479G= MANE Select	NP_054860.1:n.1348+479G=