Canonical Allele Identifier: CA2637974158

Gene: CNTNAP1

Linked Data

• gnomAD v4: 17-42687423-G-GGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42687423_42687424insGCC , CM000679.2:g.42687423_42687424insGCC	GRCh38
NC_000017.10:g.40839441_40839442insGCC , CM000679.1:g.40839441_40839442insGCC	GRCh37
NC_000017.9:g.38092967_38092968insGCC	NCBI36
NG_042091.1:g.9810_9811insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1045-297_1045-296insGCC MANE Select	ENSP00000264638.3:n.1045-297_1045-296insGCC
ENST00000264638.8:c.1045-297_1045-296insGCC	ENSP00000264638.3:n.1045-297_1045-296insGCC
ENST00000586801.1:n.163_164insGCC
ENST00000591662.1:c.1045-297_1045-296insGCC	ENSP00000466571.1:n.1045-297_1045-296insGCC
NM_003632.2:c.1045-297_1045-296insGCC	NP_003623.1:n.1045-297_1045-296insGCC
XM_005257748.3:c.817-297_817-296insGCC	XP_005257805.1:n.817-297_817-296insGCC
XM_005257748.4:c.817-297_817-296insGCC	XP_005257805.1:n.817-297_817-296insGCC
XM_017025238.1:c.1045-297_1045-296insGCC	XP_016880727.1:n.1045-297_1045-296insGCC
XM_024451011.1:c.1045-297_1045-296insGCC	XP_024306779.1:n.1045-297_1045-296insGCC
NM_003632.3:c.1045-297_1045-296insGCC MANE Select	NP_003623.1:n.1045-297_1045-296insGCC