Canonical Allele Identifier: CA2580612296
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 2530348
ClinVar RCV Id: RCV003242378

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.111410074_111410766del , CM000685.2:g.111410074_111410766del GRCh38
NC_000023.10:g.110653302_110653994del , CM000685.1:g.110653302_110653994del GRCh37
NC_000023.9:g.110539958_110540650del NCBI36
NG_011750.1:g.6414_7106del

Transcript Alleles

HGVS Amino-acid change
ENST00000706842.1:c.-23+134_326del
ENST00000356220.8:c.-22-345_326del
ENST00000358070.10:c.-34_326del
ENST00000468911.2:c.-22-345_326del
ENST00000488120.2:c.-22-345_326del
ENST00000496551.2:c.-34_326del
ENST00000635795.1:c.-22-345_326del
ENST00000636035.2:c.-22-345_326del
ENST00000637453.1:c.-22-345_326del
ENST00000637570.1:c.-22-345_326del
ENST00000338081.7:c.210_569del
ENST00000356220.7:c.-22-345_326del
ENST00000358070.8:c.185_544del
ENST00000371993.6:c.-22-345_326del
ENST00000468911.1:c.-22-345_326del
ENST00000488120.1:c.-22-345_326del
ENST00000496551.1:n.219-345_566del
NM_000555.3:c.210_569del
NM_001195553.1:c.-22-345_326del
NM_178151.2:c.-22-345_326del
NM_178152.2:c.-22-345_326del
NM_178153.2:c.-22-345_326del
XM_011530878.1:c.-22-345_326del
XM_011530879.1:c.-22-345_326del
XM_011530880.1:c.-22-345_326del
XM_011530878.3:c.-22-345_326del
XM_011530879.3:c.-22-345_326del
XM_011530880.3:c.-22-345_326del
XM_017029312.2:c.-22-345_326del
NM_001195553.2:c.-22-345_326del
NM_001369370.1:c.-22-345_326del
NM_001369371.1:c.-22-345_326del
NM_001369372.1:c.-22-345_326del
NM_001369373.1:c.-22-345_326del
NM_001369374.1:c.-22-345_326del
NM_178152.3:c.-22-345_326del
NM_178153.3:c.-22-345_326del
NM_178151.3:c.-22-345_326del