Canonical Allele Identifier: CA2260596059

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs2052949861
• gnomAD v4: 17-42682653-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682660_42682661del , CM000679.2:g.42682660_42682661del	GRCh38
NC_000017.10:g.40834678_40834679del , CM000679.1:g.40834678_40834679del	GRCh37
NC_000017.9:g.38088204_38088205del	NCBI36
NG_042091.1:g.5047_5048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-170_-169del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-170_-169del
ENST00000264638.8:c.-170_-169del (CNTNAP1)	ENSP00000264638.3:n.-170_-169del
ENST00000591568.1:c.-643+1161_-643+1162del (CCR10)	ENSP00000467331.1:n.-643+1161_-643+1162del
ENST00000591765.1:c.-977_-976del (CCR10)	ENSP00000468135.1:n.-977_-976del
NM_003632.2:c.-170_-169del (CNTNAP1)	NP_003623.1:n.-170_-169del
XM_005257748.4:c.-1190_-1189del (CNTNAP1)	XP_005257805.1:n.-1190_-1189del
XM_017025238.1:c.-170_-169del (CNTNAP1)	XP_016880727.1:n.-170_-169del
XM_024451011.1:c.-170_-169del (CNTNAP1)	XP_024306779.1:n.-170_-169del
NM_003632.3:c.-170_-169del (CNTNAP1) MANE Select	NP_003623.1:n.-170_-169del