Canonical Allele Identifier: CA171926
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 82052
dbSNP Id: rs267606317

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.111410094C>T , CM000685.2:g.111410094C>T GRCh38
NC_000023.10:g.110653322C>T , CM000685.1:g.110653322C>T GRCh37
NC_000023.9:g.110539978C>T NCBI36
NG_011750.1:g.7085G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706842.1:c.305G>A ENSP00000516583.1:p.Arg102His
ENST00000356220.8:c.305G>A ENSP00000348553.4:p.Arg102His
ENST00000358070.10:c.305G>A ENSP00000350776.5:p.Arg102His
ENST00000371993.7:c.305G>A ENSP00000361061.3:p.Arg102His
ENST00000468911.2:c.305G>A ENSP00000418811.2:p.Arg102His
ENST00000488120.2:c.305G>A ENSP00000419861.1:p.Arg102His
ENST00000496551.2:c.305G>A ENSP00000490448.1:p.Arg102His
ENST00000635795.1:c.305G>A ENSP00000489635.1:p.Arg102His
ENST00000636035.2:c.305G>A MANE Select ENSP00000490614.1:p.Arg102His
ENST00000636381.2:c.305G>A ENSP00000490068.2:p.Arg102His
ENST00000637453.1:c.305G>A ENSP00000490357.1:p.Arg102His
ENST00000637570.1:c.305G>A ENSP00000490878.1:p.Arg102His
ENST00000680476.1:c.305G>A ENSP00000505501.1:p.Arg102His
ENST00000338081.7:c.548G>A ENSP00000337697.3:p.Arg183His
ENST00000356220.7:c.305G>A ENSP00000348553.3:p.Arg102His
ENST00000358070.8:c.523G>A
ENST00000371993.6:c.305G>A ENSP00000361061.2:p.Arg102His
ENST00000468911.1:c.305G>A ENSP00000418811.1:p.Arg102His
ENST00000488120.1:c.305G>A ENSP00000419861.1:p.Arg102His
ENST00000496551.1:n.545G>A
NM_000555.3:c.548G>A NP_000546.2:p.Arg183His
NM_001195553.1:c.305G>A NP_001182482.1:p.Arg102His
NM_178151.2:c.305G>A NP_835364.1:p.Arg102His
NM_178152.2:c.305G>A NP_835365.1:p.Arg102His
NM_178153.2:c.305G>A NP_835366.1:p.Arg102His
XM_011530878.1:c.305G>A XP_011529180.1:p.Arg102His
XM_011530879.1:c.305G>A XP_011529181.1:p.Arg102His
XM_011530880.1:c.305G>A XP_011529182.1:p.Arg102His
XM_011530878.3:c.305G>A XP_011529180.1:p.Arg102His
XM_011530879.3:c.305G>A XP_011529181.1:p.Arg102His
XM_011530880.3:c.305G>A XP_011529182.1:p.Arg102His
XM_017029312.2:c.305G>A XP_016884801.1:p.Arg102His
NM_001195553.2:c.305G>A MANE Select NP_001182482.1:p.Arg102His
NM_001369370.1:c.305G>A NP_001356299.1:p.Arg102His
NM_001369371.1:c.305G>A NP_001356300.1:p.Arg102His
NM_001369372.1:c.305G>A NP_001356301.1:p.Arg102His
NM_001369373.1:c.305G>A NP_001356302.1:p.Arg102His
NM_001369374.1:c.305G>A NP_001356303.1:p.Arg102His
NM_178152.3:c.305G>A NP_835365.1:p.Arg102His
NM_178153.3:c.305G>A NP_835366.1:p.Arg102His
NM_178151.3:c.305G>A NP_835364.1:p.Arg102His