Canonical Allele Identifier: CA168784007

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs35075235

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147882680del , CM000669.2:g.147882680del	GRCh38
NC_000007.13:g.147579772del , CM000669.1:g.147579772del	GRCh37
NC_000007.12:g.147210705del	NCBI36
NG_007092.2:g.1771320del
NG_007092.3:g.1771680del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-20885del MANE Select	ENSP00000354778.3:n.2099-20885del
ENST00000636870.1:n.1961-20885del
ENST00000637825.1:n.1582-20885del
ENST00000361727.7:c.2099-20885del	ENSP00000354778.3:n.2099-20885del
ENST00000455301.2:n.34-20885del
ENST00000627772.2:n.272-20885del
NM_014141.5:c.2099-20885del	NP_054860.1:n.2099-20885del
XM_006715919.1:c.587-20885del	XP_006715982.1:n.587-20885del
NM_014141.6:c.2099-20885del MANE Select	NP_054860.1:n.2099-20885del