Canonical Allele Identifier: CA2637988675

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682649-AGAAAAGAGAGAGGAGAGACAGAGCGCTTGGGGGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682654_42682687del , CM000679.2:g.42682654_42682687del	GRCh38
NC_000017.10:g.40834672_40834705del , CM000679.1:g.40834672_40834705del	GRCh37
NC_000017.9:g.38088198_38088231del	NCBI36
NG_042091.1:g.5041_5074del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-176_-143del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-176_-143del
ENST00000264638.8:c.-176_-143del (CNTNAP1)	ENSP00000264638.3:n.-176_-143del
ENST00000591568.1:c.-643+1133_-643+1166del (CCR10)	ENSP00000467331.1:n.-643+1133_-643+1166del
ENST00000591765.1:c.-1005_-972del (CCR10)	ENSP00000468135.1:n.-1005_-972del
NM_003632.2:c.-176_-143del (CNTNAP1)	NP_003623.1:n.-176_-143del
XM_005257748.4:c.-1196_-1163del (CNTNAP1)	XP_005257805.1:n.-1196_-1163del
XM_017025238.1:c.-176_-143del (CNTNAP1)	XP_016880727.1:n.-176_-143del
XM_024451011.1:c.-176_-143del (CNTNAP1)	XP_024306779.1:n.-176_-143del
NM_003632.3:c.-176_-143del (CNTNAP1) MANE Select	NP_003623.1:n.-176_-143del