Canonical Allele Identifier: CA171866

Gene: DCX

Linked Data

• ClinVar Variation Id: 158433
• ClinVar RCV Id: RCV000145814 ; RCV001857504
• dbSNP Id: rs122457137
• COSMIC: COSM174958
• MyVariant Identifiers: chrX:g.110653451C>T (hg19) ; chrX:g.111410223C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.111410223C>T , CM000685.2:g.111410223C>T	GRCh38
NC_000023.10:g.110653451C>T , CM000685.1:g.110653451C>T	GRCh37
NC_000023.9:g.110540107C>T	NCBI36
NG_011750.1:g.6956G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706842.1:c.176G>A	ENSP00000516583.1:p.Arg59His
ENST00000356220.8:c.176G>A	ENSP00000348553.4:p.Arg59His
ENST00000358070.10:c.176G>A	ENSP00000350776.5:p.Arg59His
ENST00000371993.7:c.176G>A	ENSP00000361061.3:p.Arg59His
ENST00000468911.2:c.176G>A	ENSP00000418811.2:p.Arg59His
ENST00000488120.2:c.176G>A	ENSP00000419861.1:p.Arg59His
ENST00000496551.2:c.176G>A	ENSP00000490448.1:p.Arg59His
ENST00000635795.1:c.176G>A	ENSP00000489635.1:p.Arg59His
ENST00000636035.2:c.176G>A MANE Select	ENSP00000490614.1:p.Arg59His
ENST00000636381.2:c.176G>A	ENSP00000490068.2:p.Arg59His
ENST00000637453.1:c.176G>A	ENSP00000490357.1:p.Arg59His
ENST00000637570.1:c.176G>A	ENSP00000490878.1:p.Arg59His
ENST00000680476.1:c.176G>A	ENSP00000505501.1:p.Arg59His
ENST00000338081.7:c.419G>A	ENSP00000337697.3:p.Arg140His
ENST00000356220.7:c.176G>A	ENSP00000348553.3:p.Arg59His
ENST00000358070.8:c.394G>A
ENST00000371993.6:c.176G>A	ENSP00000361061.2:p.Arg59His
ENST00000468911.1:c.176G>A	ENSP00000418811.1:p.Arg59His
ENST00000488120.1:c.176G>A	ENSP00000419861.1:p.Arg59His
ENST00000496551.1:n.416G>A
NM_000555.3:c.419G>A	NP_000546.2:p.Arg140His
NM_001195553.1:c.176G>A	NP_001182482.1:p.Arg59His
NM_178151.2:c.176G>A	NP_835364.1:p.Arg59His
NM_178152.2:c.176G>A	NP_835365.1:p.Arg59His
NM_178153.2:c.176G>A	NP_835366.1:p.Arg59His
XM_011530878.1:c.176G>A	XP_011529180.1:p.Arg59His
XM_011530879.1:c.176G>A	XP_011529181.1:p.Arg59His
XM_011530880.1:c.176G>A	XP_011529182.1:p.Arg59His
XM_011530878.3:c.176G>A	XP_011529180.1:p.Arg59His
XM_011530879.3:c.176G>A	XP_011529181.1:p.Arg59His
XM_011530880.3:c.176G>A	XP_011529182.1:p.Arg59His
XM_017029312.2:c.176G>A	XP_016884801.1:p.Arg59His
NM_001195553.2:c.176G>A MANE Select	NP_001182482.1:p.Arg59His
NM_001369370.1:c.176G>A	NP_001356299.1:p.Arg59His
NM_001369371.1:c.176G>A	NP_001356300.1:p.Arg59His
NM_001369372.1:c.176G>A	NP_001356301.1:p.Arg59His
NM_001369373.1:c.176G>A	NP_001356302.1:p.Arg59His
NM_001369374.1:c.176G>A	NP_001356303.1:p.Arg59His
NM_178152.3:c.176G>A	NP_835365.1:p.Arg59His
NM_178153.3:c.176G>A	NP_835366.1:p.Arg59His
NM_178151.3:c.176G>A	NP_835364.1:p.Arg59His