Canonical Allele Identifier: CA2260596028

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs2052948826
• gnomAD v4: 17-42682612-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682612_42682613insC , CM000679.2:g.42682612_42682613insC	GRCh38
NC_000017.10:g.40834630_40834631insC , CM000679.1:g.40834630_40834631insC	GRCh37
NC_000017.9:g.38088156_38088157insC	NCBI36
NG_042091.1:g.4999_5000insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-218_-217insC (CNTNAP1) MANE Select	ENSP00000264638.3:n.-218_-217insC
ENST00000264638.8:c.-217-1_-217insC (CNTNAP1)	ENSP00000264638.3:n.-217-1_-217insC
ENST00000591568.1:c.-643+1203_-643+1204insG (CCR10)	ENSP00000467331.1:n.-643+1203_-643+1204insG
ENST00000591765.1:c.-935_-934insG (CCR10)	ENSP00000468135.1:n.-935_-934insG
XM_017025238.1:c.-218_-217insC (CNTNAP1)	XP_016880727.1:n.-218_-217insC
XM_024451011.1:c.-218_-217insC (CNTNAP1)	XP_024306779.1:n.-218_-217insC
NM_003632.3:c.-218_-217insC (CNTNAP1) MANE Select	NP_003623.1:n.-218_-217insC