Canonical Allele Identifier: CA2576506468

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906047del , CM000680.2:g.52906047del	GRCh38
NC_000018.9:g.50432417del , CM000680.1:g.50432417del	GRCh37
NC_000018.8:g.48686415del	NCBI36
NG_013341.1:g.570876del
NG_013341.2:g.570876del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.416del MANE Select	ENSP00000389140.2:p.Pro139HisfsTer2
ENST00000304775.12:c.217del
ENST00000412726.5:c.347del	ENSP00000397322.2:p.Pro116HisfsTer2
ENST00000442544.6:c.416del	ENSP00000389140.2:p.Pro139HisfsTer2
ENST00000579349.1:c.337del
ENST00000580024.1:n.329del
ENST00000581559.1:c.337del	ENSP00000463463.1:n.337del
NM_005215.3:c.416del	NP_005206.2:p.Pro139HisfsTer2
XM_011525843.1:c.416del	XP_011524145.1:p.Pro139HisfsTer2
XM_011525845.1:c.416del	XP_011524147.1:p.Pro139HisfsTer2
XM_011525846.1:c.416del	XP_011524148.1:p.Pro139HisfsTer2
XM_017025568.1:c.416del	XP_016881057.1:p.Pro139HisfsTer2
XM_017025569.1:c.416del	XP_016881058.1:p.Pro139HisfsTer2
NM_005215.4:c.416del MANE Select	NP_005206.2:p.Pro139HisfsTer2