Canonical Allele Identifier: CA402518149
Gene: DCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53207725A>C , CM000680.2:g.53207725A>C GRCh38
NC_000018.9:g.50734095A>C , CM000680.1:g.50734095A>C GRCh37
NC_000018.8:g.48988093A>C NCBI36
NG_013341.1:g.872554A>C
NG_013341.2:g.872554A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.1769A>C MANE Select ENSP00000389140.2:p.Lys590Thr
ENST00000304775.12:c.1570A>C
ENST00000412726.5:c.1700A>C ENSP00000397322.2:p.Lys567Thr
ENST00000442544.6:c.1769A>C ENSP00000389140.2:p.Lys590Thr
ENST00000581580.5:c.734A>C ENSP00000464582.1:p.Lys245Thr
NM_005215.3:c.1769A>C NP_005206.2:p.Lys590Thr
XM_011525843.1:c.1769A>C XP_011524145.1:p.Lys590Thr
XM_011525844.1:c.734A>C XP_011524146.1:p.Lys245Thr
XM_011525845.1:c.1769A>C XP_011524147.1:p.Lys590Thr
XM_011525846.1:c.1769A>C XP_011524148.1:p.Lys590Thr
XM_011525844.2:c.734A>C XP_011524146.1:p.Lys245Thr
XM_017025568.1:c.1769A>C XP_016881057.1:p.Lys590Thr
XM_017025569.1:c.1769A>C XP_016881058.1:p.Lys590Thr
XM_017025570.1:c.734A>C XP_016881059.1:p.Lys245Thr
NM_005215.4:c.1769A>C MANE Select NP_005206.2:p.Lys590Thr