Canonical Allele Identifier: CA2304037601
Gene: DCC HGNC NCBI

Linked Data

dbSNP Id: rs2055677295

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53207798_53207799insCCAAAACT , CM000680.2:g.53207798_53207799insCCAAAACT GRCh38
NC_000018.9:g.50734168_50734169insCCAAAACT , CM000680.1:g.50734168_50734169insCCAAAACT GRCh37
NC_000018.8:g.48988166_48988167insCCAAAACT NCBI36
NG_013341.1:g.872627_872628insCCAAAACT
NG_013341.2:g.872627_872628insCCAAAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.1842_1843insCCAAAACT MANE Select ENSP00000389140.2:p.Val615ProfsTer?
ENST00000304775.12:c.1643_1644insCCAAAACT
ENST00000412726.5:c.1773_1774insCCAAAACT ENSP00000397322.2:p.Val592ProfsTer?
ENST00000442544.6:c.1842_1843insCCAAAACT ENSP00000389140.2:p.Val615ProfsTer?
ENST00000581580.5:c.807_808insCCAAAACT ENSP00000464582.1:p.Val270ProfsTer?
NM_005215.3:c.1842_1843insCCAAAACT NP_005206.2:p.Val615ProfsTer?
XM_011525843.1:c.1842_1843insCCAAAACT XP_011524145.1:p.Val615ProfsTer?
XM_011525844.1:c.807_808insCCAAAACT XP_011524146.1:p.Val270ProfsTer?
XM_011525845.1:c.1842_1843insCCAAAACT XP_011524147.1:p.Val615ProfsTer?
XM_011525846.1:c.1842_1843insCCAAAACT XP_011524148.1:p.Val615ProfsTer?
XM_011525844.2:c.807_808insCCAAAACT XP_011524146.1:p.Val270ProfsTer?
XM_017025568.1:c.1842_1843insCCAAAACT XP_016881057.1:p.Val615ProfsTer?
XM_017025569.1:c.1842_1843insCCAAAACT XP_016881058.1:p.Val615ProfsTer?
XM_017025570.1:c.807_808insCCAAAACT XP_016881059.1:p.Val270ProfsTer?
NM_005215.4:c.1842_1843insCCAAAACT MANE Select NP_005206.2:p.Val615ProfsTer?