Canonical Allele Identifier: CA1750992610
Gene: CNTNAP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147882428T= , CM000669.2:g.147882428T= GRCh38
NC_000007.13:g.147579520T= , CM000669.1:g.147579520T= GRCh37
NC_000007.12:g.147210453T= NCBI36
NG_007092.2:g.1771068T=
NG_007092.3:g.1771428T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.2099-21137T= MANE Select ENSP00000354778.3:n.2099-21137T=
ENST00000636870.1:n.1961-21137T=
ENST00000637825.1:n.1582-21137T=
ENST00000361727.7:c.2099-21137T= ENSP00000354778.3:n.2099-21137T=
ENST00000455301.2:n.34-21137T=
ENST00000627772.2:n.272-21137T=
NM_014141.5:c.2099-21137T= NP_054860.1:n.2099-21137T=
XM_006715919.1:c.587-21137T= XP_006715982.1:n.587-21137T=
NM_014141.6:c.2099-21137T= MANE Select NP_054860.1:n.2099-21137T=
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