Canonical Allele Identifier: CA2304203609

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53530928A= , CM000680.2:g.53530928A=	GRCh38
NC_000018.9:g.51057298A= , CM000680.1:g.51057298A=	GRCh37
NC_000018.8:g.49311296A=	NCBI36
NG_013341.1:g.1195757A=
NG_013341.2:g.1195757A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.*275A= MANE Select	NP_005206.2:n.*275A=
ENST00000442544.7:c.*275A= MANE Select	ENSP00000389140.2:n.*275A=
NM_005215.3:c.*275A=	NP_005206.2:n.*275A=
ENST00000412726.5:c.4550A=	ENSP00000397322.2:n.4550A=
ENST00000442544.6:c.*275A=	ENSP00000389140.2:n.*275A=
XM_011525844.1:c.*275A=	XP_011524146.1:n.*275A=
XM_011525844.2:c.*275A=	XP_011524146.1:n.*275A=
XM_017025568.1:c.*275A=	XP_016881057.1:n.*275A=
XM_017025569.1:c.*275A=	XP_016881058.1:n.*275A=
XM_017025570.1:c.*275A=	XP_016881059.1:n.*275A=