Canonical Allele Identifier: CA1750987885

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1319243637

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147877729_147877733del , CM000669.2:g.147877729_147877733del	GRCh38
NC_000007.13:g.147574821_147574825del , CM000669.1:g.147574821_147574825del	GRCh37
NC_000007.12:g.147205754_147205758del	NCBI36
NG_007092.2:g.1766369_1766373del
NG_007092.3:g.1766729_1766733del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-25836_2099-25832del MANE Select	ENSP00000354778.3:n.2099-25836_2099-25832del
ENST00000636870.1:n.1961-25836_1961-25832del
ENST00000637825.1:n.1582-25836_1582-25832del
ENST00000361727.7:c.2099-25836_2099-25832del	ENSP00000354778.3:n.2099-25836_2099-25832del
ENST00000455301.2:n.34-25836_34-25832del
ENST00000627772.2:n.272-25836_272-25832del
NM_014141.5:c.2099-25836_2099-25832del	NP_054860.1:n.2099-25836_2099-25832del
XM_006715919.1:c.587-25836_587-25832del	XP_006715982.1:n.587-25836_587-25832del
NM_014141.6:c.2099-25836_2099-25832del MANE Select	NP_054860.1:n.2099-25836_2099-25832del