Canonical Allele Identifier: CA2260596016

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682602_42682606delinsGGATA , CM000679.2:g.42682602_42682606delinsGGATA	GRCh38
NC_000017.10:g.40834620_40834624delinsGGATA , CM000679.1:g.40834620_40834624delinsGGATA	GRCh37
NC_000017.9:g.38088146_38088150delinsGGATA	NCBI36
NG_042091.1:g.4989_4993delinsGGATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-228_-224delinsGGATA (CNTNAP1) MANE Select	ENSP00000264638.3:n.-228_-224delinsGGATA
ENST00000591568.1:c.-643+1210_-643+1214delinsTATCC (CCR10)	ENSP00000467331.1:n.-643+1210_-643+1214delinsTATCC
ENST00000591765.1:c.-928_-924delinsTATCC (CCR10)	ENSP00000468135.1:n.-928_-924delinsTATCC
XM_017025238.1:c.-228_-224delinsGGATA (CNTNAP1)	XP_016880727.1:n.-228_-224delinsGGATA
XM_024451011.1:c.-228_-224delinsGGATA (CNTNAP1)	XP_024306779.1:n.-228_-224delinsGGATA
NM_003632.3:c.-228_-224delinsGGATA (CNTNAP1) MANE Select	NP_003623.1:n.-228_-224delinsGGATA