Canonical Allele Identifier: CA369924811
Gene: CNTNAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132414A>G , CM000669.2:g.147132414A>G GRCh38
NC_000007.13:g.146829506A>G , CM000669.1:g.146829506A>G GRCh37
NC_000007.12:g.146460439A>G NCBI36
NG_007092.2:g.1021054A>G
NG_007092.3:g.1021414A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1253A>G MANE Select ENSP00000354778.3:p.Asn418Ser
ENST00000636561.1:n.1156A>G
ENST00000636870.1:n.1115A>G
ENST00000637150.1:n.1182A>G
ENST00000637694.1:n.1156A>G
ENST00000637825.1:n.736A>G
ENST00000638117.1:n.1156A>G
ENST00000361727.7:c.1253A>G ENSP00000354778.3:p.Asn418Ser
NM_014141.5:c.1253A>G NP_054860.1:p.Asn418Ser
XM_017011950.2:c.1253A>G XP_016867439.1:p.Asn418Ser
NM_014141.6:c.1253A>G MANE Select NP_054860.1:p.Asn418Ser