Canonical Allele Identifier: CA2260598493

Gene: CNTNAP1

Linked Data

• dbSNP Id: rs1734268266

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42687687_42687688insTGAATTCCCAGCTG , CM000679.2:g.42687687_42687688insTGAATTCCCAGCTG	GRCh38
NC_000017.10:g.40839705_40839706insTGAATTCCCAGCTG , CM000679.1:g.40839705_40839706insTGAATTCCCAGCTG	GRCh37
NC_000017.9:g.38093231_38093232insTGAATTCCCAGCTG	NCBI36
NG_042091.1:g.10074_10075insTGAATTCCCAGCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1045-33_1045-32insTGAATTCCCAGCTG MANE Select	ENSP00000264638.3:n.1045-33_1045-32insTGAATTCCCAGCTG
ENST00000264638.8:c.1045-33_1045-32insTGAATTCCCAGCTG	ENSP00000264638.3:n.1045-33_1045-32insTGAATTCCCAGCTG
ENST00000586801.1:n.427_428insTGAATTCCCAGCTG
ENST00000591662.1:c.1045-33_1045-32insTGAATTCCCAGCTG	ENSP00000466571.1:n.1045-33_1045-32insTGAATTCCCAGCTG
NM_003632.2:c.1045-33_1045-32insTGAATTCCCAGCTG	NP_003623.1:n.1045-33_1045-32insTGAATTCCCAGCTG
XM_005257748.3:c.817-33_817-32insTGAATTCCCAGCTG	XP_005257805.1:n.817-33_817-32insTGAATTCCCAGCTG
XM_005257748.4:c.817-33_817-32insTGAATTCCCAGCTG	XP_005257805.1:n.817-33_817-32insTGAATTCCCAGCTG
XM_017025238.1:c.1045-33_1045-32insTGAATTCCCAGCTG	XP_016880727.1:n.1045-33_1045-32insTGAATTCCCAGCTG
XM_024451011.1:c.1045-33_1045-32insTGAATTCCCAGCTG	XP_024306779.1:n.1045-33_1045-32insTGAATTCCCAGCTG
NM_003632.3:c.1045-33_1045-32insTGAATTCCCAGCTG MANE Select	NP_003623.1:n.1045-33_1045-32insTGAATTCCCAGCTG