Canonical Allele Identifier: CA1750993475
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147904596C= , CM000669.2:g.147904596C= GRCh38
NC_000007.13:g.147601688C= , CM000669.1:g.147601688C= GRCh37
NC_000007.12:g.147232621C= NCBI36
NG_007092.2:g.1793236C=
NG_007092.3:g.1793596C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.2255+875C= MANE Select ENSP00000354778.3:n.2255+875C=
ENST00000636870.1:n.2117+875C=
ENST00000637825.1:n.1738+875C=
ENST00000361727.7:c.2255+875C= ENSP00000354778.3:n.2255+875C=
ENST00000455301.2:n.190+875C=
ENST00000627772.2:n.428+875C=
NM_014141.5:c.2255+875C= NP_054860.1:n.2255+875C=
XM_006715919.1:c.743+875C= XP_006715982.1:n.743+875C=
NM_014141.6:c.2255+875C= MANE Select NP_054860.1:n.2255+875C=