Canonical Allele Identifier: CA834914630

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1381780861
• MyVariant Identifiers: chr7:g.147579863_147579887del (hg19) ; chr7:g.147882771_147882795del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147882771_147882795del , CM000669.2:g.147882771_147882795del	GRCh38
NC_000007.13:g.147579863_147579887del , CM000669.1:g.147579863_147579887del	GRCh37
NC_000007.12:g.147210796_147210820del	NCBI36
NG_007092.2:g.1771411_1771435del
NG_007092.3:g.1771771_1771795del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-20794_2099-20770del MANE Select	ENSP00000354778.3:n.2099-20794_2099-20770del
ENST00000636870.1:n.1961-20794_1961-20770del
ENST00000637825.1:n.1582-20794_1582-20770del
ENST00000361727.7:c.2099-20794_2099-20770del	ENSP00000354778.3:n.2099-20794_2099-20770del
ENST00000455301.2:n.34-20794_34-20770del
ENST00000627772.2:n.272-20794_272-20770del
NM_014141.5:c.2099-20794_2099-20770del	NP_054860.1:n.2099-20794_2099-20770del
XM_006715919.1:c.587-20794_587-20770del	XP_006715982.1:n.587-20794_587-20770del
NM_014141.6:c.2099-20794_2099-20770del MANE Select	NP_054860.1:n.2099-20794_2099-20770del