Canonical Allele Identifier: CA1750443768
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146792538A= , CM000669.2:g.146792538A= GRCh38
NC_000007.13:g.146489630A= , CM000669.1:g.146489630A= GRCh37
NC_000007.12:g.146120563A= NCBI36
NG_007092.2:g.681178A=
NG_007092.3:g.681538A=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.208+18157A= MANE Select ENSP00000354778.3:n.208+18157A=
ENST00000636561.1:n.111+18157A=
ENST00000637150.1:n.137+18157A=
ENST00000637694.1:n.111+18157A=
ENST00000638117.1:n.111+18157A=
ENST00000361727.7:c.208+18157A= ENSP00000354778.3:n.208+18157A=
ENST00000625365.2:c.208+18157A= ENSP00000485955.1:n.208+18157A=
NM_014141.5:c.208+18157A= NP_054860.1:n.208+18157A=
XM_017011950.2:c.208+18157A= XP_016867439.1:n.208+18157A=
NM_014141.6:c.208+18157A= MANE Select NP_054860.1:n.208+18157A=