Canonical Allele Identifier: CA369924587
Gene: CNTNAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132309A>T , CM000669.2:g.147132309A>T GRCh38
NC_000007.13:g.146829401A>T , CM000669.1:g.146829401A>T GRCh37
NC_000007.12:g.146460334A>T NCBI36
NG_007092.2:g.1020949A>T
NG_007092.3:g.1021309A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1148A>T MANE Select ENSP00000354778.3:p.Tyr383Phe
ENST00000636561.1:n.1051A>T
ENST00000636870.1:n.1010A>T
ENST00000637150.1:n.1077A>T
ENST00000637694.1:n.1051A>T
ENST00000637825.1:n.631A>T
ENST00000638117.1:n.1051A>T
ENST00000361727.7:c.1148A>T ENSP00000354778.3:p.Tyr383Phe
NM_014141.5:c.1148A>T NP_054860.1:p.Tyr383Phe
XM_017011950.2:c.1148A>T XP_016867439.1:p.Tyr383Phe
NM_014141.6:c.1148A>T MANE Select NP_054860.1:p.Tyr383Phe