Canonical Allele Identifier: CA1750987858

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147877723_147877725delinsTGG , CM000669.2:g.147877723_147877725delinsTGG	GRCh38
NC_000007.13:g.147574815_147574817delinsTGG , CM000669.1:g.147574815_147574817delinsTGG	GRCh37
NC_000007.12:g.147205748_147205750delinsTGG	NCBI36
NG_007092.2:g.1766363_1766365delinsTGG
NG_007092.3:g.1766723_1766725delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-25842_2099-25840delinsTGG MANE Select	ENSP00000354778.3:n.2099-25842_2099-25840delinsTGG
ENST00000636870.1:n.1961-25842_1961-25840delinsTGG
ENST00000637825.1:n.1582-25842_1582-25840delinsTGG
ENST00000361727.7:c.2099-25842_2099-25840delinsTGG	ENSP00000354778.3:n.2099-25842_2099-25840delinsTGG
ENST00000455301.2:n.34-25842_34-25840delinsTGG
ENST00000627772.2:n.272-25842_272-25840delinsTGG
NM_014141.5:c.2099-25842_2099-25840delinsTGG	NP_054860.1:n.2099-25842_2099-25840delinsTGG
XM_006715919.1:c.587-25842_587-25840delinsTGG	XP_006715982.1:n.587-25842_587-25840delinsTGG
NM_014141.6:c.2099-25842_2099-25840delinsTGG MANE Select	NP_054860.1:n.2099-25842_2099-25840delinsTGG