Canonical Allele Identifier: CA2303921705

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52991406T= , CM000680.2:g.52991406T=	GRCh38
NC_000018.9:g.50517776T= , CM000680.1:g.50517776T=	GRCh37
NC_000018.8:g.48771774T=	NCBI36
NG_013341.1:g.656235T=
NG_013341.2:g.656235T=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.985+66036T= MANE Select	NP_005206.2:n.985+66036T=
ENST00000442544.7:c.985+66036T= MANE Select	ENSP00000389140.2:n.985+66036T=
NM_005215.3:c.985+66036T=	NP_005206.2:n.985+66036T=
ENST00000304775.12:c.786+66036T=
ENST00000412726.5:c.916+66036T=	ENSP00000397322.2:n.916+66036T=
ENST00000442544.6:c.985+66036T=	ENSP00000389140.2:n.985+66036T=
ENST00000578949.1:c.-51+56516T=	ENSP00000463766.1:n.-51+56516T=
ENST00000579883.1:n.196+66036T=
ENST00000580146.1:n.237+50241T=
ENST00000581580.5:c.-51+26280T=	ENSP00000464582.1:n.-51+26280T=
XM_011525843.1:c.985+66036T=	XP_011524145.1:n.985+66036T=
XM_011525844.1:c.-51+26280T=	XP_011524146.1:n.-51+26280T=
XM_011525844.2:c.-51+26280T=	XP_011524146.1:n.-51+26280T=
XM_011525845.1:c.985+66036T=	XP_011524147.1:n.985+66036T=
XM_011525846.1:c.985+66036T=	XP_011524148.1:n.985+66036T=
XM_017025568.1:c.985+66036T=	XP_016881057.1:n.985+66036T=
XM_017025569.1:c.985+66036T=	XP_016881058.1:n.985+66036T=
XM_017025570.1:c.-51+26280T=	XP_016881059.1:n.-51+26280T=