Canonical Allele Identifier: CA2541774780
Gene: DCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52665961_52665962insGGTAGTAAACTA , CM000680.2:g.52665961_52665962insGGTAGTAAACTA GRCh38
NC_000018.9:g.50192331_50192332insGGTAGTAAACTA , CM000680.1:g.50192331_50192332insGGTAGTAAACTA GRCh37
NC_000018.8:g.48446329_48446330insGGTAGTAAACTA NCBI36
NG_013341.1:g.330790_330791insGGTAGTAAACTA
NG_013341.2:g.330790_330791insGGTAGTAAACTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.92-86093_92-86092insGGTAGTAAACTA MANE Select ENSP00000389140.2:n.92-86093_92-86092insGGTAGTAAACTA
ENST00000442544.6:c.92-86093_92-86092insGGTAGTAAACTA ENSP00000389140.2:n.92-86093_92-86092insGGTAGTAAACTA
NM_005215.3:c.92-86093_92-86092insGGTAGTAAACTA NP_005206.2:n.92-86093_92-86092insGGTAGTAAACTA
XM_011525843.1:c.92-86093_92-86092insGGTAGTAAACTA XP_011524145.1:n.92-86093_92-86092insGGTAGTAAACTA
XM_011525845.1:c.92-86093_92-86092insGGTAGTAAACTA XP_011524147.1:n.92-86093_92-86092insGGTAGTAAACTA
XM_011525846.1:c.92-86093_92-86092insGGTAGTAAACTA XP_011524148.1:n.92-86093_92-86092insGGTAGTAAACTA
XM_017025568.1:c.92-86093_92-86092insGGTAGTAAACTA XP_016881057.1:n.92-86093_92-86092insGGTAGTAAACTA
XM_017025569.1:c.92-86093_92-86092insGGTAGTAAACTA XP_016881058.1:n.92-86093_92-86092insGGTAGTAAACTA
NM_005215.4:c.92-86093_92-86092insGGTAGTAAACTA MANE Select NP_005206.2:n.92-86093_92-86092insGGTAGTAAACTA