Canonical Allele Identifier: CA2778344491

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147882770_147882793del , CM000669.2:g.147882770_147882793del	GRCh38
NC_000007.13:g.147579862_147579885del , CM000669.1:g.147579862_147579885del	GRCh37
NC_000007.12:g.147210795_147210818del	NCBI36
NG_007092.2:g.1771410_1771433del
NG_007092.3:g.1771770_1771793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-20795_2099-20772del MANE Select	ENSP00000354778.3:n.2099-20795_2099-20772del
ENST00000636870.1:n.1961-20795_1961-20772del
ENST00000637825.1:n.1582-20795_1582-20772del
ENST00000361727.7:c.2099-20795_2099-20772del	ENSP00000354778.3:n.2099-20795_2099-20772del
ENST00000455301.2:n.34-20795_34-20772del
ENST00000627772.2:n.272-20795_272-20772del
NM_014141.5:c.2099-20795_2099-20772del	NP_054860.1:n.2099-20795_2099-20772del
XM_006715919.1:c.587-20795_587-20772del	XP_006715982.1:n.587-20795_587-20772del
NM_014141.6:c.2099-20795_2099-20772del MANE Select	NP_054860.1:n.2099-20795_2099-20772del