Canonical Allele Identifier: CA2260598687

Gene: CNTNAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42688132G= , CM000679.2:g.42688132G=	GRCh38
NC_000017.10:g.40840150G= , CM000679.1:g.40840150G=	GRCh37
NC_000017.9:g.38093676G=	NCBI36
NG_042091.1:g.10519G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1306+151G= MANE Select	ENSP00000264638.3:n.1306+151G=
ENST00000264638.8:c.1306+151G=	ENSP00000264638.3:n.1306+151G=
ENST00000586801.1:n.721+151G=
ENST00000591662.1:c.1306+151G=	ENSP00000466571.1:n.1306+151G=
NM_003632.2:c.1306+151G=	NP_003623.1:n.1306+151G=
XM_005257748.3:c.1078+151G=	XP_005257805.1:n.1078+151G=
XM_005257748.4:c.1078+151G=	XP_005257805.1:n.1078+151G=
XM_017025238.1:c.1306+151G=	XP_016880727.1:n.1306+151G=
XM_024451011.1:c.1306+151G=	XP_024306779.1:n.1306+151G=
NM_003632.3:c.1306+151G= MANE Select	NP_003623.1:n.1306+151G=