Canonical Allele Identifier: CA1750987907

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1799446873

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147877736_147877737del , CM000669.2:g.147877736_147877737del	GRCh38
NC_000007.13:g.147574828_147574829del , CM000669.1:g.147574828_147574829del	GRCh37
NC_000007.12:g.147205761_147205762del	NCBI36
NG_007092.2:g.1766376_1766377del
NG_007092.3:g.1766736_1766737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-25829_2099-25828del MANE Select	ENSP00000354778.3:n.2099-25829_2099-25828del
ENST00000636870.1:n.1961-25829_1961-25828del
ENST00000637825.1:n.1582-25829_1582-25828del
ENST00000361727.7:c.2099-25829_2099-25828del	ENSP00000354778.3:n.2099-25829_2099-25828del
ENST00000455301.2:n.34-25829_34-25828del
ENST00000627772.2:n.272-25829_272-25828del
NM_014141.5:c.2099-25829_2099-25828del	NP_054860.1:n.2099-25829_2099-25828del
XM_006715919.1:c.587-25829_587-25828del	XP_006715982.1:n.587-25829_587-25828del
NM_014141.6:c.2099-25829_2099-25828del MANE Select	NP_054860.1:n.2099-25829_2099-25828del