Canonical Allele Identifier: CA402516983

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53063373T>C , CM000680.2:g.53063373T>C	GRCh38
NC_000018.9:g.50589743T>C , CM000680.1:g.50589743T>C	GRCh37
NC_000018.8:g.48843741T>C	NCBI36
NG_013341.1:g.728202T>C
NG_013341.2:g.728202T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.1054T>C MANE Select	ENSP00000389140.2:p.Cys352Arg
ENST00000304775.12:c.855T>C
ENST00000412726.5:c.985T>C	ENSP00000397322.2:p.Cys329Arg
ENST00000442544.6:c.1054T>C	ENSP00000389140.2:p.Cys352Arg
ENST00000578949.1:c.19T>C	ENSP00000463766.1:p.Cys7Arg
ENST00000579883.1:n.265T>C
ENST00000580146.1:n.306T>C
ENST00000581580.5:c.19T>C	ENSP00000464582.1:p.Cys7Arg
NM_005215.3:c.1054T>C	NP_005206.2:p.Cys352Arg
XM_011525843.1:c.1054T>C	XP_011524145.1:p.Cys352Arg
XM_011525844.1:c.19T>C	XP_011524146.1:p.Cys7Arg
XM_011525845.1:c.1054T>C	XP_011524147.1:p.Cys352Arg
XM_011525846.1:c.1054T>C	XP_011524148.1:p.Cys352Arg
XM_011525844.2:c.19T>C	XP_011524146.1:p.Cys7Arg
XM_017025568.1:c.1054T>C	XP_016881057.1:p.Cys352Arg
XM_017025569.1:c.1054T>C	XP_016881058.1:p.Cys352Arg
XM_017025570.1:c.19T>C	XP_016881059.1:p.Cys7Arg
NM_005215.4:c.1054T>C MANE Select	NP_005206.2:p.Cys352Arg