Canonical Allele Identifier: CA1108448338

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1798612143

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147491682A>C , CM000669.2:g.147491682A>C	GRCh38
NC_000007.13:g.147188774A>C , CM000669.1:g.147188774A>C	GRCh37
NC_000007.12:g.146819707A>C	NCBI36
NG_007092.2:g.1380322A>C
NG_007092.3:g.1380682A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1777+5641A>C MANE Select	ENSP00000354778.3:n.1777+5641A>C
ENST00000636870.1:n.1639+5641A>C
ENST00000637694.1:n.1681-4939A>C
ENST00000637825.1:n.1260+5641A>C
ENST00000638117.1:n.1680+5641A>C
ENST00000361727.7:c.1777+5641A>C	ENSP00000354778.3:n.1777+5641A>C
NM_014141.5:c.1777+5641A>C	NP_054860.1:n.1777+5641A>C
XM_006715919.1:c.265+5641A>C	XP_006715982.1:n.265+5641A>C
XM_017011950.2:c.1777+5641A>C	XP_016867439.1:n.1777+5641A>C
NM_014141.6:c.1777+5641A>C MANE Select	NP_054860.1:n.1777+5641A>C