Canonical Allele Identifier: CA601684046

Gene: CUL5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108041372G>A , CM000673.2:g.108041372G>A	GRCh38
NC_000011.9:g.107912099G>A , CM000673.1:g.107912099G>A	GRCh37
NC_000011.8:g.107417309G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003478.6:c.135-4898G>A MANE Select	NP_003469.2:n.135-4898G>A
ENST00000393094.7:c.135-4898G>A MANE Select	ENSP00000376808.2:n.135-4898G>A
NM_003478.3:c.135-4898G>A	NP_003469.2:n.135-4898G>A
NM_003478.4:c.135-4898G>A	NP_003469.2:n.135-4898G>A
NM_003478.5:c.135-4898G>A	NP_003469.2:n.135-4898G>A
ENST00000393094.6:c.135-4898G>A	ENSP00000376808.2:n.135-4898G>A
ENST00000526303.1:n.528-4898G>A
ENST00000531427.5:c.135-4898G>A	ENSP00000435376.1:n.135-4898G>A
ENST00000532064.5:c.134+7461G>A	ENSP00000436494.1:n.134+7461G>A
XM_005271682.2:c.135-4898G>A	XP_005271739.1:n.135-4898G>A
XM_011543013.1:c.135-4898G>A	XP_011541315.1:n.135-4898G>A
XM_011543013.2:c.135-4898G>A	XP_011541315.1:n.135-4898G>A
XM_017018363.2:c.135-4898G>A	XP_016873852.1:n.135-4898G>A
XM_017018364.1:c.-782-4898G>A	XP_016873853.1:n.-782-4898G>A
XM_017018365.1:c.-834-4898G>A	XP_016873854.1:n.-834-4898G>A