Canonical Allele Identifier: CA918157390

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs150605645

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147877724_147877725delinsT , CM000669.2:g.147877724_147877725delinsT	GRCh38
NC_000007.13:g.147574816_147574817delinsT , CM000669.1:g.147574816_147574817delinsT	GRCh37
NC_000007.12:g.147205749_147205750delinsT	NCBI36
NG_007092.2:g.1766364_1766365delinsT
NG_007092.3:g.1766724_1766725delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-25841_2099-25840delinsT MANE Select	ENSP00000354778.3:n.2099-25841_2099-25840delinsT
ENST00000636870.1:n.1961-25841_1961-25840delinsT
ENST00000637825.1:n.1582-25841_1582-25840delinsT
ENST00000361727.7:c.2099-25841_2099-25840delinsT	ENSP00000354778.3:n.2099-25841_2099-25840delinsT
ENST00000455301.2:n.34-25841_34-25840delinsT
ENST00000627772.2:n.272-25841_272-25840delinsT
NM_014141.5:c.2099-25841_2099-25840delinsT	NP_054860.1:n.2099-25841_2099-25840delinsT
XM_006715919.1:c.587-25841_587-25840delinsT	XP_006715982.1:n.587-25841_587-25840delinsT
NM_014141.6:c.2099-25841_2099-25840delinsT MANE Select	NP_054860.1:n.2099-25841_2099-25840delinsT