Canonical Allele Identifier: CA2303749694
Gene: DCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52666026C>A , CM000680.2:g.52666026C>A GRCh38
NC_000018.9:g.50192396C>A , CM000680.1:g.50192396C>A GRCh37
NC_000018.8:g.48446394C>A NCBI36
NG_013341.1:g.330855C>A
NG_013341.2:g.330855C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.92-86028C>A MANE Select ENSP00000389140.2:n.92-86028C>A
ENST00000442544.6:c.92-86028C>A ENSP00000389140.2:n.92-86028C>A
NM_005215.3:c.92-86028C>A NP_005206.2:n.92-86028C>A
XM_011525843.1:c.92-86028C>A XP_011524145.1:n.92-86028C>A
XM_011525845.1:c.92-86028C>A XP_011524147.1:n.92-86028C>A
XM_011525846.1:c.92-86028C>A XP_011524148.1:n.92-86028C>A
XM_017025568.1:c.92-86028C>A XP_016881057.1:n.92-86028C>A
XM_017025569.1:c.92-86028C>A XP_016881058.1:n.92-86028C>A
NM_005215.4:c.92-86028C>A MANE Select NP_005206.2:n.92-86028C>A