Canonical Allele Identifier: CA2260596145
Gene: CNTNAP1 HGNC NCBI
CCR10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682824_42682831delinsCCCTGCAT , CM000679.2:g.42682824_42682831delinsCCCTGCAT GRCh38
NC_000017.10:g.40834842_40834849delinsCCCTGCAT , CM000679.1:g.40834842_40834849delinsCCCTGCAT GRCh37
NC_000017.9:g.38088368_38088375delinsCCCTGCAT NCBI36
NG_042091.1:g.5211_5218delinsCCCTGCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.-6_2delinsCCCTGCAT (CNTNAP1)
ENST00000264638.8:c.-6_2delinsCCCTGCAT (CNTNAP1)
ENST00000591568.1:c.-643+985_-643+992delinsATGCAGGG (CCR10) ENSP00000467331.1:n.-643+985_-643+992delinsATGCAGGG
ENST00000591662.1:c.-6_2delinsCCCTGCAT (CNTNAP1)
ENST00000591765.1:c.-1153_-1146delinsATGCAGGG (CCR10) ENSP00000468135.1:n.-1153_-1146delinsATGCAGGG
NM_003632.2:c.-6_2delinsCCCTGCAT (CNTNAP1)
XM_005257748.4:c.-1026_-1019delinsCCCTGCAT (CNTNAP1) XP_005257805.1:n.-1026_-1019delinsCCCTGCAT
XM_017025238.1:c.-6_2delinsCCCTGCAT (CNTNAP1)
XM_024451011.1:c.-6_2delinsCCCTGCAT (CNTNAP1)
NM_003632.3:c.-6_2delinsCCCTGCAT (CNTNAP1)