Canonical Allele Identifier: CA2260598724

Gene: CNTNAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42688188_42688189delinsAG , CM000679.2:g.42688188_42688189delinsAG	GRCh38
NC_000017.10:g.40840206_40840207delinsAG , CM000679.1:g.40840206_40840207delinsAG	GRCh37
NC_000017.9:g.38093732_38093733delinsAG	NCBI36
NG_042091.1:g.10575_10576delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1306+207_1306+208delinsAG MANE Select	ENSP00000264638.3:n.1306+207_1306+208delinsAG
ENST00000264638.8:c.1306+207_1306+208delinsAG	ENSP00000264638.3:n.1306+207_1306+208delinsAG
ENST00000586801.1:n.721+207_721+208delinsAG
ENST00000591662.1:c.1306+207_1306+208delinsAG	ENSP00000466571.1:n.1306+207_1306+208delinsAG
NM_003632.2:c.1306+207_1306+208delinsAG	NP_003623.1:n.1306+207_1306+208delinsAG
XM_005257748.3:c.1078+207_1078+208delinsAG	XP_005257805.1:n.1078+207_1078+208delinsAG
XM_005257748.4:c.1078+207_1078+208delinsAG	XP_005257805.1:n.1078+207_1078+208delinsAG
XM_017025238.1:c.1306+207_1306+208delinsAG	XP_016880727.1:n.1306+207_1306+208delinsAG
XM_024451011.1:c.1306+207_1306+208delinsAG	XP_024306779.1:n.1306+207_1306+208delinsAG
NM_003632.3:c.1306+207_1306+208delinsAG MANE Select	NP_003623.1:n.1306+207_1306+208delinsAG