Canonical Allele Identifier: CA2304037599

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53207798A= , CM000680.2:g.53207798A=	GRCh38
NC_000018.9:g.50734168A= , CM000680.1:g.50734168A=	GRCh37
NC_000018.8:g.48988166A=	NCBI36
NG_013341.1:g.872627A=
NG_013341.2:g.872627A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.1842A= MANE Select	ENSP00000389140.2:p.Thr614=
ENST00000304775.12:c.1643A=
ENST00000412726.5:c.1773A=	ENSP00000397322.2:p.Thr591=
ENST00000442544.6:c.1842A=	ENSP00000389140.2:p.Thr614=
ENST00000581580.5:c.807A=	ENSP00000464582.1:p.Thr269=
NM_005215.3:c.1842A=	NP_005206.2:p.Thr614=
XM_011525843.1:c.1842A=	XP_011524145.1:p.Thr614=
XM_011525844.1:c.807A=	XP_011524146.1:p.Thr269=
XM_011525845.1:c.1842A=	XP_011524147.1:p.Thr614=
XM_011525846.1:c.1842A=	XP_011524148.1:p.Thr614=
XM_011525844.2:c.807A=	XP_011524146.1:p.Thr269=
XM_017025568.1:c.1842A=	XP_016881057.1:p.Thr614=
XM_017025569.1:c.1842A=	XP_016881058.1:p.Thr614=
XM_017025570.1:c.807A=	XP_016881059.1:p.Thr269=
NM_005215.4:c.1842A= MANE Select	NP_005206.2:p.Thr614=