Canonical Allele Identifier: CA990377648
Gene: DCC HGNC NCBI

Linked Data

dbSNP Id: rs1907553777

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53379451A>G , CM000680.2:g.53379451A>G GRCh38
NC_000018.9:g.50905821A>G , CM000680.1:g.50905821A>G GRCh37
NC_000018.8:g.49159819A>G NCBI36
NG_013341.1:g.1044280A>G
NG_013341.2:g.1044280A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.2360-6592A>G MANE Select ENSP00000389140.2:n.2360-6592A>G
ENST00000304775.12:c.2161-6592A>G
ENST00000412726.5:c.2291-6592A>G ENSP00000397322.2:n.2291-6592A>G
ENST00000442544.6:c.2360-6592A>G ENSP00000389140.2:n.2360-6592A>G
ENST00000581580.5:c.1325-6592A>G ENSP00000464582.1:n.1325-6592A>G
NM_005215.3:c.2360-6592A>G NP_005206.2:n.2360-6592A>G
XM_011525843.1:c.2360-6592A>G XP_011524145.1:n.2360-6592A>G
XM_011525844.1:c.1325-6592A>G XP_011524146.1:n.1325-6592A>G
XM_011525845.1:c.2360-6592A>G XP_011524147.1:n.2360-6592A>G
XM_011525846.1:c.2360-6592A>G XP_011524148.1:n.2360-6592A>G
XM_011525844.2:c.1325-6592A>G XP_011524146.1:n.1325-6592A>G
XM_017025568.1:c.2360-6592A>G XP_016881057.1:n.2360-6592A>G
XM_017025569.1:c.2360-6592A>G XP_016881058.1:n.2360-6592A>G
XM_017025570.1:c.1325-6592A>G XP_016881059.1:n.1325-6592A>G
NM_005215.4:c.2360-6592A>G MANE Select NP_005206.2:n.2360-6592A>G