Canonical Allele Identifier: CA2637974396

Gene: CNTNAP1

Linked Data

• gnomAD v4: 17-42687687-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42687687_42687688insT , CM000679.2:g.42687687_42687688insT	GRCh38
NC_000017.10:g.40839705_40839706insT , CM000679.1:g.40839705_40839706insT	GRCh37
NC_000017.9:g.38093231_38093232insT	NCBI36
NG_042091.1:g.10074_10075insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1045-33_1045-32insT MANE Select	ENSP00000264638.3:n.1045-33_1045-32insT
ENST00000264638.8:c.1045-33_1045-32insT	ENSP00000264638.3:n.1045-33_1045-32insT
ENST00000586801.1:n.427_428insT
ENST00000591662.1:c.1045-33_1045-32insT	ENSP00000466571.1:n.1045-33_1045-32insT
NM_003632.2:c.1045-33_1045-32insT	NP_003623.1:n.1045-33_1045-32insT
XM_005257748.3:c.817-33_817-32insT	XP_005257805.1:n.817-33_817-32insT
XM_005257748.4:c.817-33_817-32insT	XP_005257805.1:n.817-33_817-32insT
XM_017025238.1:c.1045-33_1045-32insT	XP_016880727.1:n.1045-33_1045-32insT
XM_024451011.1:c.1045-33_1045-32insT	XP_024306779.1:n.1045-33_1045-32insT
NM_003632.3:c.1045-33_1045-32insT MANE Select	NP_003623.1:n.1045-33_1045-32insT