Canonical Allele Identifier: CA1750992896
Gene: CNTNAP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147882786G= , CM000669.2:g.147882786G= GRCh38
NC_000007.13:g.147579878G= , CM000669.1:g.147579878G= GRCh37
NC_000007.12:g.147210811G= NCBI36
NG_007092.2:g.1771426G=
NG_007092.3:g.1771786G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.2099-20779G= MANE Select ENSP00000354778.3:n.2099-20779G=
ENST00000636870.1:n.1961-20779G=
ENST00000637825.1:n.1582-20779G=
ENST00000361727.7:c.2099-20779G= ENSP00000354778.3:n.2099-20779G=
ENST00000455301.2:n.34-20779G=
ENST00000627772.2:n.272-20779G=
NM_014141.5:c.2099-20779G= NP_054860.1:n.2099-20779G=
XM_006715919.1:c.587-20779G= XP_006715982.1:n.587-20779G=
NM_014141.6:c.2099-20779G= MANE Select NP_054860.1:n.2099-20779G=
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