Canonical Allele Identifier: CA350826518

Gene: CUL3

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224502964C>A , CM000664.2:g.224502964C>A	GRCh38
NC_000002.11:g.225367681C>A , CM000664.1:g.225367681C>A	GRCh37
NC_000002.10:g.225075925C>A	NCBI36
NG_032169.1:g.87434G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1485+1G>T MANE Select	ENSP00000264414.4:n.1485+1G>T
ENST00000264414.8:c.1485+1G>T	ENSP00000264414.4:n.1485+1G>T
ENST00000344951.8:c.1287+1G>T	ENSP00000343601.4:n.1287+1G>T
ENST00000409096.5:c.1413+1G>T	ENSP00000387200.1:n.1413+1G>T
ENST00000409777.5:c.1413+1G>T	ENSP00000386525.1:n.1413+1G>T
ENST00000617432.4:c.207+1G>T	ENSP00000477851.1:n.207+1G>T
NM_001257197.1:c.1287+1G>T	NP_001244126.1:n.1287+1G>T
NM_001257198.1:c.1503+1G>T	NP_001244127.1:n.1503+1G>T
NM_003590.4:c.1485+1G>T	NP_003581.1:n.1485+1G>T
XM_006712800.2:c.1452+1G>T	XP_006712863.2:n.1452+1G>T
XM_011511994.1:c.1338+1G>T	XP_011510296.1:n.1338+1G>T
XM_011511995.1:c.1443+1G>T	XP_011510297.1:n.1443+1G>T
XM_011511996.1:c.1293+1G>T	XP_011510298.1:n.1293+1G>T
XM_011511997.1:c.1185+1G>T	XP_011510299.1:n.1185+1G>T
XM_011511994.3:c.1338+1G>T	XP_011510296.1:n.1338+1G>T
XM_011511996.2:c.1293+1G>T	XP_011510298.1:n.1293+1G>T
NM_003590.5:c.1485+1G>T MANE Select	NP_003581.1:n.1485+1G>T
NM_001257198.2:c.1503+1G>T	NP_001244127.1:n.1503+1G>T
NM_001257197.2:c.1287+1G>T	NP_001244126.1:n.1287+1G>T