Canonical Allele Identifier: CA2260596095

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682723_42682730delinsAGCGGTCT , CM000679.2:g.42682723_42682730delinsAGCGGTCT	GRCh38
NC_000017.10:g.40834741_40834748delinsAGCGGTCT , CM000679.1:g.40834741_40834748delinsAGCGGTCT	GRCh37
NC_000017.9:g.38088267_38088274delinsAGCGGTCT	NCBI36
NG_042091.1:g.5110_5117delinsAGCGGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-107_-100delinsAGCGGTCT (CNTNAP1) MANE Select	ENSP00000264638.3:n.-107_-100delinsAGCGGTCT
ENST00000264638.8:c.-107_-100delinsAGCGGTCT (CNTNAP1)	ENSP00000264638.3:n.-107_-100delinsAGCGGTCT
ENST00000591568.1:c.-643+1086_-643+1093delinsAGACCGCT (CCR10)	ENSP00000467331.1:n.-643+1086_-643+1093delinsAGACCGCT
ENST00000591662.1:c.-107_-100delinsAGCGGTCT (CNTNAP1)	ENSP00000466571.1:n.-107_-100delinsAGCGGTCT
ENST00000591765.1:c.-1052_-1045delinsAGACCGCT (CCR10)	ENSP00000468135.1:n.-1052_-1045delinsAGACCGCT
NM_003632.2:c.-107_-100delinsAGCGGTCT (CNTNAP1)	NP_003623.1:n.-107_-100delinsAGCGGTCT
XM_005257748.4:c.-1127_-1120delinsAGCGGTCT (CNTNAP1)	XP_005257805.1:n.-1127_-1120delinsAGCGGTCT
XM_017025238.1:c.-107_-100delinsAGCGGTCT (CNTNAP1)	XP_016880727.1:n.-107_-100delinsAGCGGTCT
XM_024451011.1:c.-107_-100delinsAGCGGTCT (CNTNAP1)	XP_024306779.1:n.-107_-100delinsAGCGGTCT
NM_003632.3:c.-107_-100delinsAGCGGTCT (CNTNAP1) MANE Select	NP_003623.1:n.-107_-100delinsAGCGGTCT