Canonical Allele Identifier: CA1750623952

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132354G= , CM000669.2:g.147132354G=	GRCh38
NC_000007.13:g.146829446G= , CM000669.1:g.146829446G=	GRCh37
NC_000007.12:g.146460379G=	NCBI36
NG_007092.2:g.1020994G=
NG_007092.3:g.1021354G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1193G= MANE Select	ENSP00000354778.3:p.Ser398=
ENST00000636561.1:n.1096G=
ENST00000636870.1:n.1055G=
ENST00000637150.1:n.1122G=
ENST00000637694.1:n.1096G=
ENST00000637825.1:n.676G=
ENST00000638117.1:n.1096G=
ENST00000361727.7:c.1193G=	ENSP00000354778.3:p.Ser398=
NM_014141.5:c.1193G=	NP_054860.1:p.Ser398=
XM_017011950.2:c.1193G=	XP_016867439.1:p.Ser398=
NM_014141.6:c.1193G= MANE Select	NP_054860.1:p.Ser398=