Canonical Allele Identifier: CA1750624276
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132418G= , CM000669.2:g.147132418G= GRCh38
NC_000007.13:g.146829510G= , CM000669.1:g.146829510G= GRCh37
NC_000007.12:g.146460443G= NCBI36
NG_007092.2:g.1021058G=
NG_007092.3:g.1021418G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1257G= MANE Select ENSP00000354778.3:p.Leu419=
ENST00000636561.1:n.1160G=
ENST00000636870.1:n.1119G=
ENST00000637150.1:n.1186G=
ENST00000637694.1:n.1160G=
ENST00000637825.1:n.740G=
ENST00000638117.1:n.1160G=
ENST00000361727.7:c.1257G= ENSP00000354778.3:p.Leu419=
NM_014141.5:c.1257G= NP_054860.1:p.Leu419=
XM_017011950.2:c.1257G= XP_016867439.1:p.Leu419=
NM_014141.6:c.1257G= MANE Select NP_054860.1:p.Leu419=