Canonical Allele Identifier: CA171941

Gene: DCX

Linked Data

• ClinVar Variation Id: 158457
• ClinVar RCV Id: RCV000145839
• dbSNP Id: rs587783545
• MyVariant Identifiers: chrX:g.110644556del (hg19) ; chrX:g.111401328del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.111401331del , CM000685.2:g.111401331del	GRCh38
NC_000023.10:g.110644559del , CM000685.1:g.110644559del	GRCh37
NC_000023.9:g.110531215del	NCBI36
NG_011750.1:g.15851del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356220.8:c.367del
ENST00000358070.10:c.367del
ENST00000371993.7:c.367del
ENST00000468911.2:c.367del
ENST00000488120.2:c.367del
ENST00000496551.2:c.367del
ENST00000635795.1:c.367del
ENST00000636035.2:c.367del
ENST00000636381.2:c.367del
ENST00000637453.1:c.367del
ENST00000637570.1:c.367del
ENST00000680476.1:c.367del
ENST00000338081.7:c.610del
ENST00000356220.7:c.367del
ENST00000358070.8:c.585del
ENST00000371993.6:c.367del
ENST00000488120.1:c.367del
ENST00000496551.1:n.607del
NM_000555.3:c.610del
NM_001195553.1:c.367del
NM_178151.2:c.367del
NM_178152.2:c.367del
NM_178153.2:c.367del
XM_011530878.1:c.367del
XM_011530879.1:c.367del
XM_011530880.1:c.367del
XM_011530878.3:c.367del
XM_011530879.3:c.367del
XM_011530880.3:c.367del
XM_017029312.2:c.367del
NM_001195553.2:c.367del
NM_001369370.1:c.367del
NM_001369371.1:c.367del
NM_001369372.1:c.367del
NM_001369373.1:c.367del
NM_001369374.1:c.367del
NM_178152.3:c.367del
NM_178153.3:c.367del
NM_178151.3:c.367del