Canonical Allele Identifier: CA2303936689
Gene: DCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53020881G>C , CM000680.2:g.53020881G>C GRCh38
NC_000018.9:g.50547251G>C , CM000680.1:g.50547251G>C GRCh37
NC_000018.8:g.48801249G>C NCBI36
NG_013341.1:g.685710G>C
NG_013341.2:g.685710G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.986-42424G>C MANE Select ENSP00000389140.2:n.986-42424G>C
ENST00000304775.12:c.787-42424G>C
ENST00000412726.5:c.917-42424G>C ENSP00000397322.2:n.917-42424G>C
ENST00000442544.6:c.986-42424G>C ENSP00000389140.2:n.986-42424G>C
ENST00000578949.1:c.-50-42424G>C ENSP00000463766.1:n.-50-42424G>C
ENST00000579883.1:n.197-42424G>C
ENST00000580146.1:n.238-42424G>C
ENST00000581580.5:c.-50-42424G>C ENSP00000464582.1:n.-50-42424G>C
NM_005215.3:c.986-42424G>C NP_005206.2:n.986-42424G>C
XM_011525843.1:c.986-42424G>C XP_011524145.1:n.986-42424G>C
XM_011525844.1:c.-50-42424G>C XP_011524146.1:n.-50-42424G>C
XM_011525845.1:c.986-42424G>C XP_011524147.1:n.986-42424G>C
XM_011525846.1:c.986-42424G>C XP_011524148.1:n.986-42424G>C
XM_011525844.2:c.-50-42424G>C XP_011524146.1:n.-50-42424G>C
XM_017025568.1:c.986-42424G>C XP_016881057.1:n.986-42424G>C
XM_017025569.1:c.986-42424G>C XP_016881058.1:n.986-42424G>C
XM_017025570.1:c.-50-42424G>C XP_016881059.1:n.-50-42424G>C
NM_005215.4:c.986-42424G>C MANE Select NP_005206.2:n.986-42424G>C