Canonical Allele Identifier: CA16044035
Gene: DCC HGNC NCBI

Linked Data

ClinVar Variation Id: 375283
ClinVar RCV Id: RCV000416322 RCV000494701
dbSNP Id: rs1057519055
MyVariant Identifiers: chr18:g.50912467G>A (hg19) chr18:g.53386097G>A (hg38)
PubMed: PMID:28250454
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53386097G>A , CM000680.2:g.53386097G>A GRCh38
NC_000018.9:g.50912467G>A , CM000680.1:g.50912467G>A GRCh37
NC_000018.8:g.49166465G>A NCBI36
NG_013341.1:g.1050926G>A
NG_013341.2:g.1050926G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000442544.7:c.2414G>A MANE Select ENSP00000389140.2:p.Gly805Glu
ENST00000304775.12:c.2215G>A
ENST00000412726.5:c.2345G>A ENSP00000397322.2:p.Gly782Glu
ENST00000442544.6:c.2414G>A ENSP00000389140.2:p.Gly805Glu
ENST00000581580.5:c.1379G>A ENSP00000464582.1:p.Gly460Glu
NM_005215.3:c.2414G>A NP_005206.2:p.Gly805Glu
XM_011525843.1:c.2414G>A XP_011524145.1:p.Gly805Glu
XM_011525844.1:c.1379G>A XP_011524146.1:p.Gly460Glu
XM_011525845.1:c.2414G>A XP_011524147.1:p.Gly805Glu
XM_011525846.1:c.2414G>A XP_011524148.1:p.Gly805Glu
XM_011525844.2:c.1379G>A XP_011524146.1:p.Gly460Glu
XM_017025568.1:c.2414G>A XP_016881057.1:p.Gly805Glu
XM_017025569.1:c.2414G>A XP_016881058.1:p.Gly805Glu
XM_017025570.1:c.1379G>A XP_016881059.1:p.Gly460Glu
NM_005215.4:c.2414G>A MANE Select NP_005206.2:p.Gly805Glu
Search 100 bp 5'
Search 100 bp 3'