Canonical Allele Identifier: CA2637988481

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682612-AGAAGAGCGGAGGAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682613_42682626del , CM000679.2:g.42682613_42682626del	GRCh38
NC_000017.10:g.40834631_40834644del , CM000679.1:g.40834631_40834644del	GRCh37
NC_000017.9:g.38088157_38088170del	NCBI36
NG_042091.1:g.5000_5013del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-217_-204del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-217_-204del
ENST00000264638.8:c.-217_-204del (CNTNAP1)	ENSP00000264638.3:n.-217_-204del
ENST00000591568.1:c.-643+1190_-643+1203del (CCR10)	ENSP00000467331.1:n.-643+1190_-643+1203del
ENST00000591765.1:c.-948_-935del (CCR10)	ENSP00000468135.1:n.-948_-935del
XM_017025238.1:c.-217_-204del (CNTNAP1)	XP_016880727.1:n.-217_-204del
XM_024451011.1:c.-217_-204del (CNTNAP1)	XP_024306779.1:n.-217_-204del
NM_003632.3:c.-217_-204del (CNTNAP1) MANE Select	NP_003623.1:n.-217_-204del