Canonical Allele Identifier: CA1750624268
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132416T= , CM000669.2:g.147132416T= GRCh38
NC_000007.13:g.146829508T= , CM000669.1:g.146829508T= GRCh37
NC_000007.12:g.146460441T= NCBI36
NG_007092.2:g.1021056T=
NG_007092.3:g.1021416T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1255T= MANE Select ENSP00000354778.3:p.Leu419=
ENST00000636561.1:n.1158T=
ENST00000636870.1:n.1117T=
ENST00000637150.1:n.1184T=
ENST00000637694.1:n.1158T=
ENST00000637825.1:n.738T=
ENST00000638117.1:n.1158T=
ENST00000361727.7:c.1255T= ENSP00000354778.3:p.Leu419=
NM_014141.5:c.1255T= NP_054860.1:p.Leu419=
XM_017011950.2:c.1255T= XP_016867439.1:p.Leu419=
NM_014141.6:c.1255T= MANE Select NP_054860.1:p.Leu419=