Canonical Allele Identifier: CA2637988227

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682542-G-GCGCCCGCTGGCTCTCATCTTTTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682542_42682543insCGCCCGCTGGCTCTCATCTTTTCC , CM000679.2:g.42682542_42682543insCGCCCGCTGGCTCTCATCTTTTCC	GRCh38
NC_000017.10:g.40834560_40834561insCGCCCGCTGGCTCTCATCTTTTCC , CM000679.1:g.40834560_40834561insCGCCCGCTGGCTCTCATCTTTTCC	GRCh37
NC_000017.9:g.38088086_38088087insCGCCCGCTGGCTCTCATCTTTTCC	NCBI36
NG_042091.1:g.4929_4930insCGCCCGCTGGCTCTCATCTTTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-288_-287insCGCCCGCTGGCTCTCATCTTTTCC (CNTNAP1) MANE Select	ENSP00000264638.3:n.-288_-287insCGCCCGCTGGCTCTCATCTTTTCC
ENST00000591568.1:c.-643+1273_-643+1274insGGAAAAGATGAGAGCCAGCGGGCG (CCR10)	ENSP00000467331.1:n.-643+1273_-643+1274insGGAAAAGATGAGAGCCAGC...
ENST00000591765.1:c.-865_-864insGGAAAAGATGAGAGCCAGCGGGCG (CCR10)	ENSP00000468135.1:n.-865_-864insGGAAAAGATGAGAGCCAGCGGGCG
XM_017025238.1:c.-288_-287insCGCCCGCTGGCTCTCATCTTTTCC (CNTNAP1)	XP_016880727.1:n.-288_-287insCGCCCGCTGGCTCTCATCTTTTCC
XM_024451011.1:c.-288_-287insCGCCCGCTGGCTCTCATCTTTTCC (CNTNAP1)	XP_024306779.1:n.-288_-287insCGCCCGCTGGCTCTCATCTTTTCC
NM_003632.3:c.-288_-287insCGCCCGCTGGCTCTCATCTTTTCC (CNTNAP1) MANE Select	NP_003623.1:n.-288_-287insCGCCCGCTGGCTCTCATCTTTTCC