Canonical Allele Identifier: CA168783380

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs368632794

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147877725delinsTT , CM000669.2:g.147877725delinsTT	GRCh38
NC_000007.13:g.147574817delinsTT , CM000669.1:g.147574817delinsTT	GRCh37
NC_000007.12:g.147205750delinsTT	NCBI36
NG_007092.2:g.1766365delinsTT
NG_007092.3:g.1766725delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-25840delinsTT MANE Select	ENSP00000354778.3:n.2099-25840delinsTT
ENST00000636870.1:n.1961-25840delinsTT
ENST00000637825.1:n.1582-25840delinsTT
ENST00000361727.7:c.2099-25840delinsTT	ENSP00000354778.3:n.2099-25840delinsTT
ENST00000455301.2:n.34-25840delinsTT
ENST00000627772.2:n.272-25840delinsTT
NM_014141.5:c.2099-25840delinsTT	NP_054860.1:n.2099-25840delinsTT
XM_006715919.1:c.587-25840delinsTT	XP_006715982.1:n.587-25840delinsTT
NM_014141.6:c.2099-25840delinsTT MANE Select	NP_054860.1:n.2099-25840delinsTT