Canonical Allele Identifier: CA2685448892
Gene: CNTNAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132375del , CM000669.2:g.147132375del GRCh38
NC_000007.13:g.146829467del , CM000669.1:g.146829467del GRCh37
NC_000007.12:g.146460400del NCBI36
NG_007092.2:g.1021015del
NG_007092.3:g.1021375del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1214del MANE Select ENSP00000354778.3:p.Asn405ThrfsTer?
ENST00000636561.1:n.1117del
ENST00000636870.1:n.1076del
ENST00000637150.1:n.1143del
ENST00000637694.1:n.1117del
ENST00000637825.1:n.697del
ENST00000638117.1:n.1117del
ENST00000361727.7:c.1214del ENSP00000354778.3:p.Asn405ThrfsTer?
NM_014141.5:c.1214del NP_054860.1:p.Asn405ThrfsTer?
XM_017011950.2:c.1214del XP_016867439.1:p.Asn405ThrfsTer?
NM_014141.6:c.1214del MANE Select NP_054860.1:p.Asn405ThrfsTer?