Canonical Allele Identifier: CA1750623859
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132311C= , CM000669.2:g.147132311C= GRCh38
NC_000007.13:g.146829403C= , CM000669.1:g.146829403C= GRCh37
NC_000007.12:g.146460336C= NCBI36
NG_007092.2:g.1020951C=
NG_007092.3:g.1021311C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1150C= MANE Select ENSP00000354778.3:p.Leu384=
ENST00000636561.1:n.1053C=
ENST00000636870.1:n.1012C=
ENST00000637150.1:n.1079C=
ENST00000637694.1:n.1053C=
ENST00000637825.1:n.633C=
ENST00000638117.1:n.1053C=
ENST00000361727.7:c.1150C= ENSP00000354778.3:p.Leu384=
NM_014141.5:c.1150C= NP_054860.1:p.Leu384=
XM_017011950.2:c.1150C= XP_016867439.1:p.Leu384=
NM_014141.6:c.1150C= MANE Select NP_054860.1:p.Leu384=