Canonical Allele Identifier: CA1750443623

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146792268_146792272delinsTAAAA , CM000669.2:g.146792268_146792272delinsTAAAA	GRCh38
NC_000007.13:g.146489360_146489364delinsTAAAA , CM000669.1:g.146489360_146489364delinsTAAAA	GRCh37
NC_000007.12:g.146120293_146120297delinsTAAAA	NCBI36
NG_007092.2:g.680908_680912delinsTAAAA
NG_007092.3:g.681268_681272delinsTAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.208+17887_208+17891delinsTAAAA MANE Select	ENSP00000354778.3:n.208+17887_208+17891delinsTAAAA
ENST00000636561.1:n.111+17887_111+17891delinsTAAAA
ENST00000637150.1:n.137+17887_137+17891delinsTAAAA
ENST00000637694.1:n.111+17887_111+17891delinsTAAAA
ENST00000638117.1:n.111+17887_111+17891delinsTAAAA
ENST00000361727.7:c.208+17887_208+17891delinsTAAAA	ENSP00000354778.3:n.208+17887_208+17891delinsTAAAA
ENST00000625365.2:c.208+17887_208+17891delinsTAAAA	ENSP00000485955.1:n.208+17887_208+17891delinsTAAAA
NM_014141.5:c.208+17887_208+17891delinsTAAAA	NP_054860.1:n.208+17887_208+17891delinsTAAAA
XM_017011950.2:c.208+17887_208+17891delinsTAAAA	XP_016867439.1:n.208+17887_208+17891delinsTAAAA
NM_014141.6:c.208+17887_208+17891delinsTAAAA MANE Select	NP_054860.1:n.208+17887_208+17891delinsTAAAA