Canonical Allele Identifier: CA3228996129

Gene: DCC

Genomic Alleles

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

Transcript Alleles

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