Canonical Allele Identifier: CA12600431
Gene: CNTNAP2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2710117

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147904680T>A , CM000669.2:g.147904680T>A GRCh38
NC_000007.12:g.147232705T>A NCBI36
NC_000007.13:g.147601772T>A , CM000669.1:g.147601772T>A GRCh37
NG_007092.2:g.1793320T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.7:c.2255+959T>A ENSP00000354778.3:p.=
ENST00000455301.2:n.190+959T>A
ENST00000627772.2:n.428+959T>A
NM_014141.5:c.2255+959T>A NP_054860.1:p.=
XM_006715919.1:c.743+959T>A XP_006715982.1:p.=