Canonical Allele Identifier: CA915950015
Gene: CNTNAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 800937
ClinVar RCV Id: RCV000985145

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682830_42689520del , CM000679.2:g.42682830_42689520del GRCh38
NG_042091.1:g.5217_11907del

Transcript Alleles

HGVS Amino-acid change
ENST00000264638.9:c.1_1629-1del
ENST00000264638.8:c.1_1629-1del
ENST00000591662.1:c.1_1629-1del
NM_003632.2:c.1_1629-1del
XM_005257748.4:c.-1020_1401-1del
XM_017025238.1:c.1_1629-1del
XM_024451011.1:c.1_1629-1del
NM_003632.3:c.1_1629-1del