Canonical Allele Identifier: CA657391675

Gene: DCC

Linked Data

• COSMIC: COSN6126756

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52665984T>C , CM000680.2:g.52665984T>C	GRCh38
NC_000018.9:g.50192354T>C , CM000680.1:g.50192354T>C	GRCh37
NC_000018.8:g.48446352T>C	NCBI36
NG_013341.1:g.330813T>C
NG_013341.2:g.330813T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.92-86070T>C MANE Select	ENSP00000389140.2:n.92-86070T>C
ENST00000442544.6:c.92-86070T>C	ENSP00000389140.2:n.92-86070T>C
NM_005215.3:c.92-86070T>C	NP_005206.2:n.92-86070T>C
XM_011525843.1:c.92-86070T>C	XP_011524145.1:n.92-86070T>C
XM_011525845.1:c.92-86070T>C	XP_011524147.1:n.92-86070T>C
XM_011525846.1:c.92-86070T>C	XP_011524148.1:n.92-86070T>C
XM_017025568.1:c.92-86070T>C	XP_016881057.1:n.92-86070T>C
XM_017025569.1:c.92-86070T>C	XP_016881058.1:n.92-86070T>C
NM_005215.4:c.92-86070T>C MANE Select	NP_005206.2:n.92-86070T>C