Canonical Allele Identifier: CA2304132167

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53391777G= , CM000680.2:g.53391777G=	GRCh38
NC_000018.9:g.50918147G= , CM000680.1:g.50918147G=	GRCh37
NC_000018.8:g.49172145G=	NCBI36
NG_013341.1:g.1056606G=
NG_013341.2:g.1056606G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.2578G= MANE Select	ENSP00000389140.2:p.Val860=
ENST00000304775.12:c.2257-5531G=
ENST00000412726.5:c.2509G=	ENSP00000397322.2:p.Val837=
ENST00000442544.6:c.2578G=	ENSP00000389140.2:p.Val860=
ENST00000581580.5:c.1483G=	ENSP00000464582.1:p.Val495=
NM_005215.3:c.2578G=	NP_005206.2:p.Val860=
XM_011525843.1:c.2578G=	XP_011524145.1:p.Val860=
XM_011525844.1:c.1543G=	XP_011524146.1:p.Val515=
XM_011525845.1:c.2578G=	XP_011524147.1:p.Val860=
XM_011525846.1:c.2518G=	XP_011524148.1:p.Val840=
XM_011525844.2:c.1543G=	XP_011524146.1:p.Val515=
XM_017025568.1:c.2578G=	XP_016881057.1:p.Val860=
XM_017025569.1:c.2518G=	XP_016881058.1:p.Val840=
XM_017025570.1:c.1543G=	XP_016881059.1:p.Val515=
NM_005215.4:c.2578G= MANE Select	NP_005206.2:p.Val860=