Canonical Allele Identifier: CA121594
Gene: DCX HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11599
dbSNP Id: rs104894781

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.111401322A>G , CM000685.2:g.111401322A>G GRCh38
NC_000023.10:g.110644550A>G , CM000685.1:g.110644550A>G GRCh37
NC_000023.9:g.110531206A>G NCBI36
NG_011750.1:g.15857T>C

Transcript Alleles

HGVS Amino-acid change
NM_000555.3:c.616T>C VV NP_000546.2:p.Tyr206His
NM_001195553.1:c.373T>C VV NP_001182482.1:p.Tyr125His
NM_178151.2:c.373T>C VV NP_835364.1:p.Tyr125His
NM_178152.2:c.373T>C VV NP_835365.1:p.Tyr125His
NM_178153.2:c.373T>C VV NP_835366.1:p.Tyr125His
XM_011530878.1:c.373T>C XP_011529180.1:p.Tyr125His
XM_011530879.1:c.373T>C XP_011529181.1:p.Tyr125His
XM_011530880.1:c.373T>C XP_011529182.1:p.Tyr125His
XM_011530878.3:c.373T>C
XM_011530879.3:c.373T>C
XM_011530880.3:c.373T>C
XM_017029312.2:c.373T>C XP_016884801.1:p.Tyr125His
ENST00000338081.7:c.616T>C ENSP00000337697.3:p.Tyr206His
ENST00000356220.7:c.373T>C ENSP00000348553.3:p.Tyr125His
ENST00000358070.8:n.591T>C
ENST00000371993.6:c.373T>C ENSP00000361061.2:p.Tyr125His
ENST00000488120.1:c.373T>C ENSP00000419861.1:p.Tyr125His
ENST00000496551.1:n.613T>C