Canonical Allele Identifier: CA1750623861
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132313G= , CM000669.2:g.147132313G= GRCh38
NC_000007.13:g.146829405G= , CM000669.1:g.146829405G= GRCh37
NC_000007.12:g.146460338G= NCBI36
NG_007092.2:g.1020953G=
NG_007092.3:g.1021313G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1152G= MANE Select ENSP00000354778.3:p.Leu384=
ENST00000636561.1:n.1055G=
ENST00000636870.1:n.1014G=
ENST00000637150.1:n.1081G=
ENST00000637694.1:n.1055G=
ENST00000637825.1:n.635G=
ENST00000638117.1:n.1055G=
ENST00000361727.7:c.1152G= ENSP00000354778.3:p.Leu384=
NM_014141.5:c.1152G= NP_054860.1:p.Leu384=
XM_017011950.2:c.1152G= XP_016867439.1:p.Leu384=
NM_014141.6:c.1152G= MANE Select NP_054860.1:p.Leu384=