Canonical Allele Identifier: CA3228996128

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52689042C>A , CM000680.2:g.52689042C>A	GRCh38
NC_000018.9:g.50215412C>A , CM000680.1:g.50215412C>A	GRCh37
NC_000018.8:g.48469410C>A	NCBI36
NG_013341.1:g.353871C>A
NG_013341.2:g.353871C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.92-63012C>A MANE Select	NP_005206.2:n.92-63012C>A
ENST00000442544.7:c.92-63012C>A MANE Select	ENSP00000389140.2:n.92-63012C>A
NM_005215.3:c.92-63012C>A	NP_005206.2:n.92-63012C>A
ENST00000442544.6:c.92-63012C>A	ENSP00000389140.2:n.92-63012C>A
XM_011525843.1:c.92-63012C>A	XP_011524145.1:n.92-63012C>A
XM_011525845.1:c.92-63012C>A	XP_011524147.1:n.92-63012C>A
XM_011525846.1:c.92-63012C>A	XP_011524148.1:n.92-63012C>A
XM_017025568.1:c.92-63012C>A	XP_016881057.1:n.92-63012C>A
XM_017025569.1:c.92-63012C>A	XP_016881058.1:n.92-63012C>A