Canonical Allele Identifier: CA1750988254
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147878052A= , CM000669.2:g.147878052A= GRCh38
NC_000007.13:g.147575144A= , CM000669.1:g.147575144A= GRCh37
NC_000007.12:g.147206077A= NCBI36
NG_007092.2:g.1766692A=
NG_007092.3:g.1767052A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.2099-25513A= MANE Select ENSP00000354778.3:n.2099-25513A=
ENST00000636870.1:n.1961-25513A=
ENST00000637825.1:n.1582-25513A=
ENST00000361727.7:c.2099-25513A= ENSP00000354778.3:n.2099-25513A=
ENST00000455301.2:n.34-25513A=
ENST00000627772.2:n.272-25513A=
NM_014141.5:c.2099-25513A= NP_054860.1:n.2099-25513A=
XM_006715919.1:c.587-25513A= XP_006715982.1:n.587-25513A=
NM_014141.6:c.2099-25513A= MANE Select NP_054860.1:n.2099-25513A=