Canonical Allele Identifier: CA2303874885

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52905782G= , CM000680.2:g.52905782G=	GRCh38
NC_000018.9:g.50432152G= , CM000680.1:g.50432152G=	GRCh37
NC_000018.8:g.48686150G=	NCBI36
NG_013341.1:g.570611G=
NG_013341.2:g.570611G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.413-262G= MANE Select	ENSP00000389140.2:n.413-262G=
ENST00000304775.12:c.214-262G=
ENST00000412726.5:c.344-262G=	ENSP00000397322.2:n.344-262G=
ENST00000442544.6:c.413-262G=	ENSP00000389140.2:n.413-262G=
ENST00000579349.1:c.334-262G=
ENST00000580024.1:n.326-262G=
ENST00000581559.1:c.334-262G=	ENSP00000463463.1:n.334-262G=
NM_005215.3:c.413-262G=	NP_005206.2:n.413-262G=
XM_011525843.1:c.413-262G=	XP_011524145.1:n.413-262G=
XM_011525845.1:c.413-262G=	XP_011524147.1:n.413-262G=
XM_011525846.1:c.413-262G=	XP_011524148.1:n.413-262G=
XM_017025568.1:c.413-262G=	XP_016881057.1:n.413-262G=
XM_017025569.1:c.413-262G=	XP_016881058.1:n.413-262G=
NM_005215.4:c.413-262G= MANE Select	NP_005206.2:n.413-262G=