Canonical Allele Identifier: CA2304180076

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53486808G= , CM000680.2:g.53486808G=	GRCh38
NC_000018.9:g.51013178G= , CM000680.1:g.51013178G=	GRCh37
NC_000018.8:g.49267176G=	NCBI36
NG_013341.1:g.1151637G=
NG_013341.2:g.1151637G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.3748G= MANE Select	NP_005206.2:p.Ala1250=
ENST00000442544.7:c.3748G= MANE Select	ENSP00000389140.2:p.Ala1250=
NM_005215.3:c.3748G=	NP_005206.2:p.Ala1250=
ENST00000412726.5:c.3679G=	ENSP00000397322.2:p.Ala1227=
ENST00000442544.6:c.3748G=	ENSP00000389140.2:p.Ala1250=
ENST00000581580.5:c.2653G=	ENSP00000464582.1:p.Ala885=
XM_011525843.1:c.3748G=	XP_011524145.1:p.Ala1250=
XM_011525844.1:c.2713G=	XP_011524146.1:p.Ala905=
XM_011525844.2:c.2713G=	XP_011524146.1:p.Ala905=
XM_017025568.1:c.3748G=	XP_016881057.1:p.Ala1250=
XM_017025569.1:c.3688G=	XP_016881058.1:p.Ala1230=
XM_017025570.1:c.2713G=	XP_016881059.1:p.Ala905=