Canonical Allele Identifier: CA2303874996
Gene: DCC HGNC NCBI

Linked Data

dbSNP Id: rs2039876639
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52906034T>A , CM000680.2:g.52906034T>A GRCh38
NC_000018.9:g.50432404T>A , CM000680.1:g.50432404T>A GRCh37
NC_000018.8:g.48686402T>A NCBI36
NG_013341.1:g.570863T>A
NG_013341.2:g.570863T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000442544.7:c.413-10T>A MANE Select ENSP00000389140.2:n.413-10T>A
ENST00000304775.12:c.214-10T>A
ENST00000412726.5:c.344-10T>A ENSP00000397322.2:n.344-10T>A
ENST00000442544.6:c.413-10T>A ENSP00000389140.2:n.413-10T>A
ENST00000579349.1:c.334-10T>A
ENST00000580024.1:n.326-10T>A
ENST00000581559.1:c.334-10T>A ENSP00000463463.1:n.334-10T>A
NM_005215.3:c.413-10T>A NP_005206.2:n.413-10T>A
XM_011525843.1:c.413-10T>A XP_011524145.1:n.413-10T>A
XM_011525845.1:c.413-10T>A XP_011524147.1:n.413-10T>A
XM_011525846.1:c.413-10T>A XP_011524148.1:n.413-10T>A
XM_017025568.1:c.413-10T>A XP_016881057.1:n.413-10T>A
XM_017025569.1:c.413-10T>A XP_016881058.1:n.413-10T>A
NM_005215.4:c.413-10T>A MANE Select NP_005206.2:n.413-10T>A
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