Canonical Allele Identifier: CA2778344488

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147882727A>T , CM000669.2:g.147882727A>T	GRCh38
NC_000007.13:g.147579819A>T , CM000669.1:g.147579819A>T	GRCh37
NC_000007.12:g.147210752A>T	NCBI36
NG_007092.2:g.1771367A>T
NG_007092.3:g.1771727A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-20838A>T MANE Select	ENSP00000354778.3:n.2099-20838A>T
ENST00000636870.1:n.1961-20838A>T
ENST00000637825.1:n.1582-20838A>T
ENST00000361727.7:c.2099-20838A>T	ENSP00000354778.3:n.2099-20838A>T
ENST00000455301.2:n.34-20838A>T
ENST00000627772.2:n.272-20838A>T
NM_014141.5:c.2099-20838A>T	NP_054860.1:n.2099-20838A>T
XM_006715919.1:c.587-20838A>T	XP_006715982.1:n.587-20838A>T
NM_014141.6:c.2099-20838A>T MANE Select	NP_054860.1:n.2099-20838A>T