Canonical Allele Identifier: CA2304170688

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53467923A= , CM000680.2:g.53467923A=	GRCh38
NC_000018.9:g.50994293A= , CM000680.1:g.50994293A=	GRCh37
NC_000018.8:g.49248291A=	NCBI36
NG_013341.1:g.1132752A=
NG_013341.2:g.1132752A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.3649A= MANE Select	NP_005206.2:p.Met1217=
ENST00000442544.7:c.3649A= MANE Select	ENSP00000389140.2:p.Met1217=
NM_005215.3:c.3649A=	NP_005206.2:p.Met1217=
ENST00000412726.5:c.3580A=	ENSP00000397322.2:p.Met1194=
ENST00000442544.6:c.3649A=	ENSP00000389140.2:p.Met1217=
ENST00000581580.5:c.2554A=	ENSP00000464582.1:p.Met852=
XM_011525843.1:c.3649A=	XP_011524145.1:p.Met1217=
XM_011525844.1:c.2614A=	XP_011524146.1:p.Met872=
XM_011525844.2:c.2614A=	XP_011524146.1:p.Met872=
XM_017025568.1:c.3649A=	XP_016881057.1:p.Met1217=
XM_017025569.1:c.3589A=	XP_016881058.1:p.Met1197=
XM_017025570.1:c.2614A=	XP_016881059.1:p.Met872=