Canonical Allele Identifier: CA171846

Gene: DCX

Linked Data

• ClinVar Variation Id: 158425
• ClinVar RCV Id: RCV000145806 ; RCV002514810 ; RCV002514809
• dbSNP Id: rs587783519
• gnomAD v4: X-111410284-G-A
• COSMIC: COSM2722025 ; COSM2722026
• MyVariant Identifiers: chrX:g.110653512G>A (hg19) ; chrX:g.111410284G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.111410284G>A , CM000685.2:g.111410284G>A	GRCh38
NC_000023.10:g.110653512G>A , CM000685.1:g.110653512G>A	GRCh37
NC_000023.9:g.110540168G>A	NCBI36
NG_011750.1:g.6895C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706842.1:c.115C>T	ENSP00000516583.1:p.Arg39Ter
ENST00000356220.8:c.115C>T	ENSP00000348553.4:p.Arg39Ter
ENST00000358070.10:c.115C>T	ENSP00000350776.5:p.Arg39Ter
ENST00000371993.7:c.115C>T	ENSP00000361061.3:p.Arg39Ter
ENST00000468911.2:c.115C>T	ENSP00000418811.2:p.Arg39Ter
ENST00000488120.2:c.115C>T	ENSP00000419861.1:p.Arg39Ter
ENST00000496551.2:c.115C>T	ENSP00000490448.1:p.Arg39Ter
ENST00000635795.1:c.115C>T	ENSP00000489635.1:p.Arg39Ter
ENST00000636035.2:c.115C>T MANE Select	ENSP00000490614.1:p.Arg39Ter
ENST00000636381.2:c.115C>T	ENSP00000490068.2:p.Arg39Ter
ENST00000637453.1:c.115C>T	ENSP00000490357.1:p.Arg39Ter
ENST00000637570.1:c.115C>T	ENSP00000490878.1:p.Arg39Ter
ENST00000680476.1:c.115C>T	ENSP00000505501.1:p.Arg39Ter
ENST00000338081.7:c.358C>T	ENSP00000337697.3:p.Arg120Ter
ENST00000356220.7:c.115C>T	ENSP00000348553.3:p.Arg39Ter
ENST00000358070.8:c.333C>T
ENST00000371993.6:c.115C>T	ENSP00000361061.2:p.Arg39Ter
ENST00000468911.1:c.115C>T	ENSP00000418811.1:p.Arg39Ter
ENST00000488120.1:c.115C>T	ENSP00000419861.1:p.Arg39Ter
ENST00000496551.1:n.355C>T
NM_000555.3:c.358C>T	NP_000546.2:p.Arg120Ter
NM_001195553.1:c.115C>T	NP_001182482.1:p.Arg39Ter
NM_178151.2:c.115C>T	NP_835364.1:p.Arg39Ter
NM_178152.2:c.115C>T	NP_835365.1:p.Arg39Ter
NM_178153.2:c.115C>T	NP_835366.1:p.Arg39Ter
XM_011530878.1:c.115C>T	XP_011529180.1:p.Arg39Ter
XM_011530879.1:c.115C>T	XP_011529181.1:p.Arg39Ter
XM_011530880.1:c.115C>T	XP_011529182.1:p.Arg39Ter
XM_011530878.3:c.115C>T	XP_011529180.1:p.Arg39Ter
XM_011530879.3:c.115C>T	XP_011529181.1:p.Arg39Ter
XM_011530880.3:c.115C>T	XP_011529182.1:p.Arg39Ter
XM_017029312.2:c.115C>T	XP_016884801.1:p.Arg39Ter
NM_001195553.2:c.115C>T MANE Select	NP_001182482.1:p.Arg39Ter
NM_001369370.1:c.115C>T	NP_001356299.1:p.Arg39Ter
NM_001369371.1:c.115C>T	NP_001356300.1:p.Arg39Ter
NM_001369372.1:c.115C>T	NP_001356301.1:p.Arg39Ter
NM_001369373.1:c.115C>T	NP_001356302.1:p.Arg39Ter
NM_001369374.1:c.115C>T	NP_001356303.1:p.Arg39Ter
NM_178152.3:c.115C>T	NP_835365.1:p.Arg39Ter
NM_178153.3:c.115C>T	NP_835366.1:p.Arg39Ter
NM_178151.3:c.115C>T	NP_835364.1:p.Arg39Ter