Canonical Allele Identifier: CA8967187
Gene: DCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1344762
ClinVar RCV Id: RCV001849763
dbSNP Id: rs181197485

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53386138G>A , CM000680.2:g.53386138G>A GRCh38
NC_000018.9:g.50912508G>A , CM000680.1:g.50912508G>A GRCh37
NC_000018.8:g.49166506G>A NCBI36
NG_013341.1:g.1050967G>A
NG_013341.2:g.1050967G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.2455G>A MANE Select ENSP00000389140.2:p.Asp819Asn
ENST00000304775.12:c.2256G>A
ENST00000412726.5:c.2386G>A ENSP00000397322.2:p.Asp796Asn
ENST00000442544.6:c.2455G>A ENSP00000389140.2:p.Asp819Asn
ENST00000581580.5:c.1420G>A ENSP00000464582.1:p.Asp474Asn
NM_005215.3:c.2455G>A NP_005206.2:p.Asp819Asn
XM_011525843.1:c.2455G>A XP_011524145.1:p.Asp819Asn
XM_011525844.1:c.1420G>A XP_011524146.1:p.Asp474Asn
XM_011525845.1:c.2455G>A XP_011524147.1:p.Asp819Asn
XM_011525846.1:c.2455G>A XP_011524148.1:p.Asp819Asn
XM_011525844.2:c.1420G>A XP_011524146.1:p.Asp474Asn
XM_017025568.1:c.2455G>A XP_016881057.1:p.Asp819Asn
XM_017025569.1:c.2455G>A XP_016881058.1:p.Asp819Asn
XM_017025570.1:c.1420G>A XP_016881059.1:p.Asp474Asn
NM_005215.4:c.2455G>A MANE Select NP_005206.2:p.Asp819Asn