Canonical Allele Identifier: CA1750805281
Gene: CNTNAP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147491687C= , CM000669.2:g.147491687C= GRCh38
NC_000007.13:g.147188779C= , CM000669.1:g.147188779C= GRCh37
NC_000007.12:g.146819712C= NCBI36
NG_007092.2:g.1380327C=
NG_007092.3:g.1380687C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1777+5646C= MANE Select ENSP00000354778.3:n.1777+5646C=
ENST00000636870.1:n.1639+5646C=
ENST00000637694.1:n.1681-4934C=
ENST00000637825.1:n.1260+5646C=
ENST00000638117.1:n.1680+5646C=
ENST00000361727.7:c.1777+5646C= ENSP00000354778.3:n.1777+5646C=
NM_014141.5:c.1777+5646C= NP_054860.1:n.1777+5646C=
XM_006715919.1:c.265+5646C= XP_006715982.1:n.265+5646C=
XM_017011950.2:c.1777+5646C= XP_016867439.1:n.1777+5646C=
NM_014141.6:c.1777+5646C= MANE Select NP_054860.1:n.1777+5646C=
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