Canonical Allele Identifier: CA2637974369

Gene: CNTNAP1

Linked Data

• gnomAD v4: 17-42687627-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42687628_42687629insTT , CM000679.2:g.42687628_42687629insTT	GRCh38
NC_000017.10:g.40839646_40839647insTT , CM000679.1:g.40839646_40839647insTT	GRCh37
NC_000017.9:g.38093172_38093173insTT	NCBI36
NG_042091.1:g.10015_10016insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1045-92_1045-91insTT MANE Select	ENSP00000264638.3:n.1045-92_1045-91insTT
ENST00000264638.8:c.1045-92_1045-91insTT	ENSP00000264638.3:n.1045-92_1045-91insTT
ENST00000586801.1:n.368_369insTT
ENST00000591662.1:c.1045-92_1045-91insTT	ENSP00000466571.1:n.1045-92_1045-91insTT
NM_003632.2:c.1045-92_1045-91insTT	NP_003623.1:n.1045-92_1045-91insTT
XM_005257748.3:c.817-92_817-91insTT	XP_005257805.1:n.817-92_817-91insTT
XM_005257748.4:c.817-92_817-91insTT	XP_005257805.1:n.817-92_817-91insTT
XM_017025238.1:c.1045-92_1045-91insTT	XP_016880727.1:n.1045-92_1045-91insTT
XM_024451011.1:c.1045-92_1045-91insTT	XP_024306779.1:n.1045-92_1045-91insTT
NM_003632.3:c.1045-92_1045-91insTT MANE Select	NP_003623.1:n.1045-92_1045-91insTT