Canonical Allele Identifier: CA16621179
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 419226
ClinVar RCV Id: RCV000478400
dbSNP Id: rs1064793735

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.111410035del , CM000685.2:g.111410035del GRCh38
NC_000023.10:g.110653263del , CM000685.1:g.110653263del GRCh37
NC_000023.9:g.110539919del NCBI36
NG_011750.1:g.7145del

Transcript Alleles

HGVS Amino-acid change
ENST00000356220.8:c.364+1del
ENST00000358070.10:c.364+1del
ENST00000371993.7:c.364+1del
ENST00000468911.2:c.364+1del
ENST00000488120.2:c.364+1del
ENST00000496551.2:c.364+1del
ENST00000635795.1:c.364+1del
ENST00000636035.2:c.364+1del
ENST00000636381.2:c.364+1del
ENST00000637453.1:c.364+1del
ENST00000637570.1:c.364+1del
ENST00000680476.1:c.364+1del
ENST00000338081.7:c.607+1del
ENST00000356220.7:c.364+1del
ENST00000358070.8:c.582+1del
ENST00000371993.6:c.364+1del
ENST00000488120.1:c.364+1del
ENST00000496551.1:n.604+1del
NM_000555.3:c.607+1del
NM_001195553.1:c.364+1del
NM_178151.2:c.364+1del
NM_178152.2:c.364+1del
NM_178153.2:c.364+1del
XM_011530878.1:c.364+1del
XM_011530879.1:c.364+1del
XM_011530880.1:c.364+1del
XM_011530878.3:c.364+1del
XM_011530879.3:c.364+1del
XM_011530880.3:c.364+1del
XM_017029312.2:c.364+1del
NM_001195553.2:c.364+1del
NM_001369370.1:c.364+1del
NM_001369371.1:c.364+1del
NM_001369372.1:c.364+1del
NM_001369373.1:c.364+1del
NM_001369374.1:c.364+1del
NM_178152.3:c.364+1del
NM_178153.3:c.364+1del
NM_178151.3:c.364+1del