Canonical Allele Identifier: CA2303749670
Gene: DCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52665994A= , CM000680.2:g.52665994A= GRCh38
NC_000018.9:g.50192364A= , CM000680.1:g.50192364A= GRCh37
NC_000018.8:g.48446362A= NCBI36
NG_013341.1:g.330823A=
NG_013341.2:g.330823A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.92-86060A= MANE Select ENSP00000389140.2:n.92-86060A=
ENST00000442544.6:c.92-86060A= ENSP00000389140.2:n.92-86060A=
NM_005215.3:c.92-86060A= NP_005206.2:n.92-86060A=
XM_011525843.1:c.92-86060A= XP_011524145.1:n.92-86060A=
XM_011525845.1:c.92-86060A= XP_011524147.1:n.92-86060A=
XM_011525846.1:c.92-86060A= XP_011524148.1:n.92-86060A=
XM_017025568.1:c.92-86060A= XP_016881057.1:n.92-86060A=
XM_017025569.1:c.92-86060A= XP_016881058.1:n.92-86060A=
NM_005215.4:c.92-86060A= MANE Select NP_005206.2:n.92-86060A=