Canonical Allele Identifier: CA2303885675

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52925310A= , CM000680.2:g.52925310A=	GRCh38
NC_000018.9:g.50451680A= , CM000680.1:g.50451680A=	GRCh37
NC_000018.8:g.48705678A=	NCBI36
NG_013341.1:g.590139A=
NG_013341.2:g.590139A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.925A= MANE Select	NP_005206.2:p.Thr309=
ENST00000442544.7:c.925A= MANE Select	ENSP00000389140.2:p.Thr309=
NM_005215.3:c.925A=	NP_005206.2:p.Thr309=
ENST00000304775.12:c.726A=
ENST00000412726.5:c.856A=	ENSP00000397322.2:p.Thr286=
ENST00000442544.6:c.925A=	ENSP00000389140.2:p.Thr309=
ENST00000579883.1:n.136A=
ENST00000584710.5:n.151A=
XM_011525843.1:c.925A=	XP_011524145.1:p.Thr309=
XM_011525845.1:c.925A=	XP_011524147.1:p.Thr309=
XM_011525846.1:c.925A=	XP_011524148.1:p.Thr309=
XM_017025568.1:c.925A=	XP_016881057.1:p.Thr309=
XM_017025569.1:c.925A=	XP_016881058.1:p.Thr309=