Canonical Allele Identifier: CA2303794284

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52759028C= , CM000680.2:g.52759028C=	GRCh38
NC_000018.9:g.50285398C= , CM000680.1:g.50285398C=	GRCh37
NC_000018.8:g.48539396C=	NCBI36
NG_013341.1:g.423857C=
NG_013341.2:g.423857C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.412+6654C= MANE Select	NP_005206.2:n.412+6654C=
ENST00000442544.7:c.412+6654C= MANE Select	ENSP00000389140.2:n.412+6654C=
NM_005215.3:c.412+6654C=	NP_005206.2:n.412+6654C=
ENST00000304775.12:c.213+6654C=
ENST00000412726.5:c.343+6654C=	ENSP00000397322.2:n.343+6654C=
ENST00000442544.6:c.412+6654C=	ENSP00000389140.2:n.412+6654C=
ENST00000578080.1:c.557C=
ENST00000579349.1:c.209+6654C=
ENST00000580024.1:n.216+6654C=
ENST00000581559.1:c.208+6654C=	ENSP00000463463.1:n.208+6654C=
ENST00000582875.1:c.214+6654C=	ENSP00000463131.1:n.214+6654C=
XM_011525843.1:c.412+6654C=	XP_011524145.1:n.412+6654C=
XM_011525845.1:c.412+6654C=	XP_011524147.1:n.412+6654C=
XM_011525846.1:c.412+6654C=	XP_011524148.1:n.412+6654C=
XM_017025568.1:c.412+6654C=	XP_016881057.1:n.412+6654C=
XM_017025569.1:c.412+6654C=	XP_016881058.1:n.412+6654C=