Canonical Allele Identifier: CA2260598580

Gene: CNTNAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42687890_42687891delinsCG , CM000679.2:g.42687890_42687891delinsCG	GRCh38
NC_000017.10:g.40839908_40839909delinsCG , CM000679.1:g.40839908_40839909delinsCG	GRCh37
NC_000017.9:g.38093434_38093435delinsCG	NCBI36
NG_042091.1:g.10277_10278delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1215_1216delinsCG MANE Select	ENSP00000264638.3:p.Asp405=
ENST00000264638.8:c.1215_1216delinsCG	ENSP00000264638.3:p.Asp405=
ENST00000586801.1:n.630_631delinsCG
ENST00000591662.1:c.1215_1216delinsCG	ENSP00000466571.1:p.Asp405=
NM_003632.2:c.1215_1216delinsCG	NP_003623.1:p.Asp405=
XM_005257748.3:c.987_988delinsCG	XP_005257805.1:p.Asp329=
XM_005257748.4:c.987_988delinsCG	XP_005257805.1:p.Asp329=
XM_017025238.1:c.1215_1216delinsCG	XP_016880727.1:p.Asp405=
XM_024451011.1:c.1215_1216delinsCG	XP_024306779.1:p.Asp405=
NM_003632.3:c.1215_1216delinsCG MANE Select	NP_003623.1:p.Asp405=