Canonical Allele Identifier: CA224225

Gene: DCX

Linked Data

• ClinVar Variation Id: 96553
• ClinVar RCV Id: RCV000082707
• dbSNP Id: rs398124557
• MyVariant Identifiers: chrX:g.110576302T>C (hg19) ; chrX:g.111333074T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.111333074T>C , CM000685.2:g.111333074T>C	GRCh38
NC_000023.10:g.110576302T>C , CM000685.1:g.110576302T>C	GRCh37
NC_000023.9:g.110462958T>C	NCBI36
NG_011750.1:g.84105A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356220.8:c.785A>G	ENSP00000348553.4:p.Asp262Gly
ENST00000358070.10:c.785A>G	ENSP00000350776.5:p.Asp262Gly
ENST00000371993.7:c.785A>G	ENSP00000361061.3:p.Asp262Gly
ENST00000468911.2:c.785A>G	ENSP00000418811.2:p.Asp262Gly
ENST00000488120.2:c.785A>G	ENSP00000419861.1:p.Asp262Gly
ENST00000496551.2:c.785A>G	ENSP00000490448.1:p.Asp262Gly
ENST00000635795.1:c.785A>G	ENSP00000489635.1:p.Asp262Gly
ENST00000636035.2:c.785A>G MANE Select	ENSP00000490614.1:p.Asp262Gly
ENST00000636381.2:c.785A>G	ENSP00000490068.2:p.Asp262Gly
ENST00000637453.1:c.785A>G	ENSP00000490357.1:p.Asp262Gly
ENST00000637570.1:c.785A>G	ENSP00000490878.1:p.Asp262Gly
ENST00000680476.1:c.785A>G	ENSP00000505501.1:p.Asp262Gly
ENST00000338081.7:c.1028A>G	ENSP00000337697.3:p.Asp343Gly
ENST00000356220.7:c.785A>G	ENSP00000348553.3:p.Asp262Gly
ENST00000358070.8:c.1003A>G
ENST00000371993.6:c.785A>G	ENSP00000361061.2:p.Asp262Gly
ENST00000488120.1:c.785A>G	ENSP00000419861.1:p.Asp262Gly
ENST00000496551.1:n.1025A>G
NM_000555.3:c.1028A>G	NP_000546.2:p.Asp343Gly
NM_001195553.1:c.785A>G	NP_001182482.1:p.Asp262Gly
NM_178151.2:c.785A>G	NP_835364.1:p.Asp262Gly
NM_178152.2:c.785A>G	NP_835365.1:p.Asp262Gly
NM_178153.2:c.785A>G	NP_835366.1:p.Asp262Gly
XM_011530878.1:c.785A>G	XP_011529180.1:p.Asp262Gly
XM_011530879.1:c.785A>G	XP_011529181.1:p.Asp262Gly
XM_011530880.1:c.785A>G	XP_011529182.1:p.Asp262Gly
XM_011530878.3:c.785A>G	XP_011529180.1:p.Asp262Gly
XM_011530879.3:c.785A>G	XP_011529181.1:p.Asp262Gly
XM_011530880.3:c.785A>G	XP_011529182.1:p.Asp262Gly
XM_017029312.2:c.785A>G	XP_016884801.1:p.Asp262Gly
NM_001195553.2:c.785A>G MANE Select	NP_001182482.1:p.Asp262Gly
NM_001369370.1:c.785A>G	NP_001356299.1:p.Asp262Gly
NM_001369371.1:c.785A>G	NP_001356300.1:p.Asp262Gly
NM_001369372.1:c.785A>G	NP_001356301.1:p.Asp262Gly
NM_001369373.1:c.785A>G	NP_001356302.1:p.Asp262Gly
NM_001369374.1:c.785A>G	NP_001356303.1:p.Asp262Gly
NM_178152.3:c.785A>G	NP_835365.1:p.Asp262Gly
NM_178153.3:c.785A>G	NP_835366.1:p.Asp262Gly
NM_178151.3:c.785A>G	NP_835364.1:p.Asp262Gly