Canonical Allele Identifier: CA2303874960

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52905962A= , CM000680.2:g.52905962A=	GRCh38
NC_000018.9:g.50432332A= , CM000680.1:g.50432332A=	GRCh37
NC_000018.8:g.48686330A=	NCBI36
NG_013341.1:g.570791A=
NG_013341.2:g.570791A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.413-82A= MANE Select	ENSP00000389140.2:n.413-82A=
ENST00000304775.12:c.214-82A=
ENST00000412726.5:c.344-82A=	ENSP00000397322.2:n.344-82A=
ENST00000442544.6:c.413-82A=	ENSP00000389140.2:n.413-82A=
ENST00000579349.1:c.334-82A=
ENST00000580024.1:n.326-82A=
ENST00000581559.1:c.334-82A=	ENSP00000463463.1:n.334-82A=
NM_005215.3:c.413-82A=	NP_005206.2:n.413-82A=
XM_011525843.1:c.413-82A=	XP_011524145.1:n.413-82A=
XM_011525845.1:c.413-82A=	XP_011524147.1:n.413-82A=
XM_011525846.1:c.413-82A=	XP_011524148.1:n.413-82A=
XM_017025568.1:c.413-82A=	XP_016881057.1:n.413-82A=
XM_017025569.1:c.413-82A=	XP_016881058.1:n.413-82A=
NM_005215.4:c.413-82A= MANE Select	NP_005206.2:n.413-82A=