Canonical Allele Identifier: CA1751005485

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147918558A= , CM000669.2:g.147918558A=	GRCh38
NC_000007.13:g.147615650A= , CM000669.1:g.147615650A=	GRCh37
NC_000007.12:g.147246583A=	NCBI36
NG_007092.2:g.1807198A=
NG_007092.3:g.1807558A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.2255+14837A= MANE Select	ENSP00000354778.3:n.2255+14837A=
ENST00000636870.1:n.2117+14837A=
ENST00000637825.1:n.1738+14837A=
ENST00000361727.7:c.2255+14837A=	ENSP00000354778.3:n.2255+14837A=
ENST00000455301.2:n.190+14837A=
ENST00000627772.2:n.428+14837A=
NM_014141.5:c.2255+14837A=	NP_054860.1:n.2255+14837A=
XM_006715919.1:c.743+14837A=	XP_006715982.1:n.743+14837A=
NM_014141.6:c.2255+14837A= MANE Select	NP_054860.1:n.2255+14837A=