Canonical Allele Identifier: CA1750624192

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132380A= , CM000669.2:g.147132380A=	GRCh38
NC_000007.13:g.146829472A= , CM000669.1:g.146829472A=	GRCh37
NC_000007.12:g.146460405A=	NCBI36
NG_007092.2:g.1021020A=
NG_007092.3:g.1021380A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1219A= MANE Select	ENSP00000354778.3:p.Asn407=
ENST00000636561.1:n.1122A=
ENST00000636870.1:n.1081A=
ENST00000637150.1:n.1148A=
ENST00000637694.1:n.1122A=
ENST00000637825.1:n.702A=
ENST00000638117.1:n.1122A=
ENST00000361727.7:c.1219A=	ENSP00000354778.3:p.Asn407=
NM_014141.5:c.1219A=	NP_054860.1:p.Asn407=
XM_017011950.2:c.1219A=	XP_016867439.1:p.Asn407=
NM_014141.6:c.1219A= MANE Select	NP_054860.1:p.Asn407=