Canonical Allele Identifier: CA2303782829

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52734641T= , CM000680.2:g.52734641T=	GRCh38
NC_000018.9:g.50261011T= , CM000680.1:g.50261011T=	GRCh37
NC_000018.8:g.48515009T=	NCBI36
NG_013341.1:g.399470T=
NG_013341.2:g.399470T=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.92-17413T= MANE Select	NP_005206.2:n.92-17413T=
ENST00000442544.7:c.92-17413T= MANE Select	ENSP00000389140.2:n.92-17413T=
NM_005215.3:c.92-17413T=	NP_005206.2:n.92-17413T=
ENST00000442544.6:c.92-17413T=	ENSP00000389140.2:n.92-17413T=
XM_011525843.1:c.92-17413T=	XP_011524145.1:n.92-17413T=
XM_011525845.1:c.92-17413T=	XP_011524147.1:n.92-17413T=
XM_011525846.1:c.92-17413T=	XP_011524148.1:n.92-17413T=
XM_017025568.1:c.92-17413T=	XP_016881057.1:n.92-17413T=
XM_017025569.1:c.92-17413T=	XP_016881058.1:n.92-17413T=