Canonical Allele Identifier: CA2303884870

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52923832C= , CM000680.2:g.52923832C=	GRCh38
NC_000018.9:g.50450202C= , CM000680.1:g.50450202C=	GRCh37
NC_000018.8:g.48704200C=	NCBI36
NG_013341.1:g.588661C=
NG_013341.2:g.588661C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.823C= MANE Select	NP_005206.2:p.Arg275=
ENST00000442544.7:c.823C= MANE Select	ENSP00000389140.2:p.Arg275=
NM_005215.3:c.823C=	NP_005206.2:p.Arg275=
ENST00000304775.12:c.624C=
ENST00000412726.5:c.754C=	ENSP00000397322.2:p.Arg252=
ENST00000442544.6:c.823C=	ENSP00000389140.2:p.Arg275=
ENST00000579883.1:n.34C=
ENST00000584710.5:n.49C=
XM_011525843.1:c.823C=	XP_011524145.1:p.Arg275=
XM_011525845.1:c.823C=	XP_011524147.1:p.Arg275=
XM_011525846.1:c.823C=	XP_011524148.1:p.Arg275=
XM_017025568.1:c.823C=	XP_016881057.1:p.Arg275=
XM_017025569.1:c.823C=	XP_016881058.1:p.Arg275=