Canonical Allele Identifier: CA2303922479

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52992904A= , CM000680.2:g.52992904A=	GRCh38
NC_000018.9:g.50519274A= , CM000680.1:g.50519274A=	GRCh37
NC_000018.8:g.48773272A=	NCBI36
NG_013341.1:g.657733A=
NG_013341.2:g.657733A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.985+67534A= MANE Select	NP_005206.2:n.985+67534A=
ENST00000442544.7:c.985+67534A= MANE Select	ENSP00000389140.2:n.985+67534A=
NM_005215.3:c.985+67534A=	NP_005206.2:n.985+67534A=
ENST00000304775.12:c.786+67534A=
ENST00000412726.5:c.916+67534A=	ENSP00000397322.2:n.916+67534A=
ENST00000442544.6:c.985+67534A=	ENSP00000389140.2:n.985+67534A=
ENST00000578949.1:c.-51+58014A=	ENSP00000463766.1:n.-51+58014A=
ENST00000579883.1:n.196+67534A=
ENST00000580146.1:n.237+51739A=
ENST00000581580.5:c.-51+27778A=	ENSP00000464582.1:n.-51+27778A=
XM_011525843.1:c.985+67534A=	XP_011524145.1:n.985+67534A=
XM_011525844.1:c.-51+27778A=	XP_011524146.1:n.-51+27778A=
XM_011525844.2:c.-51+27778A=	XP_011524146.1:n.-51+27778A=
XM_011525845.1:c.985+67534A=	XP_011524147.1:n.985+67534A=
XM_011525846.1:c.985+67534A=	XP_011524148.1:n.985+67534A=
XM_017025568.1:c.985+67534A=	XP_016881057.1:n.985+67534A=
XM_017025569.1:c.985+67534A=	XP_016881058.1:n.985+67534A=
XM_017025570.1:c.-51+27778A=	XP_016881059.1:n.-51+27778A=