Canonical Allele Identifier: CA2260596001

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682566_42682574delinsAGGGGGGAG , CM000679.2:g.42682566_42682574delinsAGGGGGGAG	GRCh38
NC_000017.10:g.40834584_40834592delinsAGGGGGGAG , CM000679.1:g.40834584_40834592delinsAGGGGGGAG	GRCh37
NC_000017.9:g.38088110_38088118delinsAGGGGGGAG	NCBI36
NG_042091.1:g.4953_4961delinsAGGGGGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-264_-256delinsAGGGGGGAG (CNTNAP1) MANE Select	ENSP00000264638.3:n.-264_-256delinsAGGGGGGAG
ENST00000591568.1:c.-643+1242_-643+1250delinsCTCCCCCCT (CCR10)	ENSP00000467331.1:n.-643+1242_-643+1250delinsCTCCCCCCT
ENST00000591765.1:c.-896_-888delinsCTCCCCCCT (CCR10)	ENSP00000468135.1:n.-896_-888delinsCTCCCCCCT
XM_017025238.1:c.-264_-256delinsAGGGGGGAG (CNTNAP1)	XP_016880727.1:n.-264_-256delinsAGGGGGGAG
XM_024451011.1:c.-264_-256delinsAGGGGGGAG (CNTNAP1)	XP_024306779.1:n.-264_-256delinsAGGGGGGAG
NM_003632.3:c.-264_-256delinsAGGGGGGAG (CNTNAP1) MANE Select	NP_003623.1:n.-264_-256delinsAGGGGGGAG