Canonical Allele Identifier: CA645618248

Gene: DCC

Linked Data

• COSMIC: COSM5205850 ; COSM5205851

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906247del , CM000680.2:g.52906247del	GRCh38
NC_000018.9:g.50432617del , CM000680.1:g.50432617del	GRCh37
NC_000018.8:g.48686615del	NCBI36
NG_013341.1:g.571076del
NG_013341.2:g.571076del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.616del MANE Select	ENSP00000389140.2:p.Asp206ThrfsTer?
ENST00000304775.12:c.417del
ENST00000412726.5:c.547del	ENSP00000397322.2:p.Asp183ThrfsTer?
ENST00000442544.6:c.616del	ENSP00000389140.2:p.Asp206ThrfsTer?
ENST00000579349.1:c.537del
ENST00000580024.1:n.529del
ENST00000581559.1:c.537del	ENSP00000463463.1:n.537del
NM_005215.3:c.616del	NP_005206.2:p.Asp206ThrfsTer?
XM_011525843.1:c.616del	XP_011524145.1:p.Asp206ThrfsTer?
XM_011525845.1:c.616del	XP_011524147.1:p.Asp206ThrfsTer?
XM_011525846.1:c.616del	XP_011524148.1:p.Asp206ThrfsTer?
XM_017025568.1:c.616del	XP_016881057.1:p.Asp206ThrfsTer?
XM_017025569.1:c.616del	XP_016881058.1:p.Asp206ThrfsTer?
NM_005215.4:c.616del MANE Select	NP_005206.2:p.Asp206ThrfsTer?