Canonical Allele Identifier: CA2303875069

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906202G= , CM000680.2:g.52906202G=	GRCh38
NC_000018.9:g.50432572G= , CM000680.1:g.50432572G=	GRCh37
NC_000018.8:g.48686570G=	NCBI36
NG_013341.1:g.571031G=
NG_013341.2:g.571031G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.571G= MANE Select	ENSP00000389140.2:p.Val191=
ENST00000304775.12:c.372G=
ENST00000412726.5:c.502G=	ENSP00000397322.2:p.Val168=
ENST00000442544.6:c.571G=	ENSP00000389140.2:p.Val191=
ENST00000579349.1:c.492G=
ENST00000580024.1:n.484G=
ENST00000581559.1:c.492G=	ENSP00000463463.1:n.492G=
NM_005215.3:c.571G=	NP_005206.2:p.Val191=
XM_011525843.1:c.571G=	XP_011524145.1:p.Val191=
XM_011525845.1:c.571G=	XP_011524147.1:p.Val191=
XM_011525846.1:c.571G=	XP_011524148.1:p.Val191=
XM_017025568.1:c.571G=	XP_016881057.1:p.Val191=
XM_017025569.1:c.571G=	XP_016881058.1:p.Val191=
NM_005215.4:c.571G= MANE Select	NP_005206.2:p.Val191=