Canonical Allele Identifier: CA1750992890

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147882772_147882796delinsCAGGACAGAACCCAGGAAATCCAAT , CM000669.2:g.147882772_147882796delinsCAGGACAGAACCCAGGAAATCCAAT	GRCh38
NC_000007.13:g.147579864_147579888delinsCAGGACAGAACCCAGGAAATCCAAT , CM000669.1:g.147579864_147579888delinsCAGGACAGAACCCAGGAAATCCAAT	GRCh37
NC_000007.12:g.147210797_147210821delinsCAGGACAGAACCCAGGAAATCCAAT	NCBI36
NG_007092.2:g.1771412_1771436delinsCAGGACAGAACCCAGGAAATCCAAT
NG_007092.3:g.1771772_1771796delinsCAGGACAGAACCCAGGAAATCCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-20793_2099-20769delinsCAGGACAGAACCCAGGAAATCCAAT MANE Select	ENSP00000354778.3:n.2099-20793_2099-20769delinsCAGGACAGAACCCA...
ENST00000636870.1:n.1961-20793_1961-20769delinsCAGGACAGAACCCAGGAAATCCAAT
ENST00000637825.1:n.1582-20793_1582-20769delinsCAGGACAGAACCCAGGAAATCCAAT
ENST00000361727.7:c.2099-20793_2099-20769delinsCAGGACAGAACCCAGGAAATCCAAT	ENSP00000354778.3:n.2099-20793_2099-20769delinsCAGGACAGAACCCA...
ENST00000455301.2:n.34-20793_34-20769delinsCAGGACAGAACCCAGGAAATCCAAT
ENST00000627772.2:n.272-20793_272-20769delinsCAGGACAGAACCCAGGAAATCCAAT
NM_014141.5:c.2099-20793_2099-20769delinsCAGGACAGAACCCAGGAAATCCAAT	NP_054860.1:n.2099-20793_2099-20769delinsCAGGACAGAACCCAGGAAAT...
XM_006715919.1:c.587-20793_587-20769delinsCAGGACAGAACCCAGGAAATCCAAT	XP_006715982.1:n.587-20793_587-20769delinsCAGGACAGAACCCAGGAAA...
NM_014141.6:c.2099-20793_2099-20769delinsCAGGACAGAACCCAGGAAATCCAAT MANE Select	NP_054860.1:n.2099-20793_2099-20769delinsCAGGACAGAACCCAGGAAAT...