Canonical Allele Identifier: CA1750436669

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146778242_146778244delinsTTA , CM000669.2:g.146778242_146778244delinsTTA	GRCh38
NC_000007.13:g.146475334_146475336delinsTTA , CM000669.1:g.146475334_146475336delinsTTA	GRCh37
NC_000007.12:g.146106267_146106269delinsTTA	NCBI36
NG_007092.2:g.666882_666884delinsTTA
NG_007092.3:g.667242_667244delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.208+3861_208+3863delinsTTA MANE Select	ENSP00000354778.3:n.208+3861_208+3863delinsTTA
ENST00000636277.1:n.75+3861_75+3863delinsTTA
ENST00000636561.1:n.111+3861_111+3863delinsTTA
ENST00000636600.1:n.58+3861_58+3863delinsTTA
ENST00000637150.1:n.137+3861_137+3863delinsTTA
ENST00000637694.1:n.111+3861_111+3863delinsTTA
ENST00000638117.1:n.111+3861_111+3863delinsTTA
ENST00000361727.7:c.208+3861_208+3863delinsTTA	ENSP00000354778.3:n.208+3861_208+3863delinsTTA
ENST00000625365.2:c.208+3861_208+3863delinsTTA	ENSP00000485955.1:n.208+3861_208+3863delinsTTA
NM_014141.5:c.208+3861_208+3863delinsTTA	NP_054860.1:n.208+3861_208+3863delinsTTA
XM_017011950.2:c.208+3861_208+3863delinsTTA	XP_016867439.1:n.208+3861_208+3863delinsTTA
NM_014141.6:c.208+3861_208+3863delinsTTA MANE Select	NP_054860.1:n.208+3861_208+3863delinsTTA