Canonical Allele Identifier: CA2304037519

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53207745C= , CM000680.2:g.53207745C=	GRCh38
NC_000018.9:g.50734115C= , CM000680.1:g.50734115C=	GRCh37
NC_000018.8:g.48988113C=	NCBI36
NG_013341.1:g.872574C=
NG_013341.2:g.872574C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.1789C= MANE Select	NP_005206.2:p.Arg597=
ENST00000442544.7:c.1789C= MANE Select	ENSP00000389140.2:p.Arg597=
NM_005215.3:c.1789C=	NP_005206.2:p.Arg597=
ENST00000304775.12:c.1590C=
ENST00000412726.5:c.1720C=	ENSP00000397322.2:p.Arg574=
ENST00000442544.6:c.1789C=	ENSP00000389140.2:p.Arg597=
ENST00000581580.5:c.754C=	ENSP00000464582.1:p.Arg252=
XM_011525843.1:c.1789C=	XP_011524145.1:p.Arg597=
XM_011525844.1:c.754C=	XP_011524146.1:p.Arg252=
XM_011525844.2:c.754C=	XP_011524146.1:p.Arg252=
XM_011525845.1:c.1789C=	XP_011524147.1:p.Arg597=
XM_011525846.1:c.1789C=	XP_011524148.1:p.Arg597=
XM_017025568.1:c.1789C=	XP_016881057.1:p.Arg597=
XM_017025569.1:c.1789C=	XP_016881058.1:p.Arg597=
XM_017025570.1:c.754C=	XP_016881059.1:p.Arg252=