Canonical Allele Identifier: CA2260596017

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs2052948575

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682605_42682608del , CM000679.2:g.42682605_42682608del	GRCh38
NC_000017.10:g.40834623_40834626del , CM000679.1:g.40834623_40834626del	GRCh37
NC_000017.9:g.38088149_38088152del	NCBI36
NG_042091.1:g.4992_4995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-225_-222del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-225_-222del
ENST00000591568.1:c.-643+1210_-643+1213del (CCR10)	ENSP00000467331.1:n.-643+1210_-643+1213del
ENST00000591765.1:c.-928_-925del (CCR10)	ENSP00000468135.1:n.-928_-925del
XM_017025238.1:c.-225_-222del (CNTNAP1)	XP_016880727.1:n.-225_-222del
XM_024451011.1:c.-225_-222del (CNTNAP1)	XP_024306779.1:n.-225_-222del
NM_003632.3:c.-225_-222del (CNTNAP1) MANE Select	NP_003623.1:n.-225_-222del