Canonical Allele Identifier: CA350827131
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503695C>A , CM000664.2:g.224503695C>A GRCh38
NC_000002.11:g.225368412C>A , CM000664.1:g.225368412C>A GRCh37
NC_000002.10:g.225076656C>A NCBI36
NG_032169.1:g.86703G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1334G>T MANE Select ENSP00000264414.4:p.Ser445Ile
ENST00000264414.8:c.1334G>T ENSP00000264414.4:p.Ser445Ile
ENST00000344951.8:c.1136G>T ENSP00000343601.4:p.Ser379Ile
ENST00000409096.5:c.1262G>T ENSP00000387200.1:p.Ser421Ile
ENST00000409777.5:c.1262G>T ENSP00000386525.1:p.Ser421Ile
ENST00000481135.1:n.630G>T
ENST00000617432.4:c.58G>T ENSP00000477851.1:p.Val20Leu
NM_001257197.1:c.1136G>T NP_001244126.1:p.Ser379Ile
NM_001257198.1:c.1352G>T NP_001244127.1:p.Ser451Ile
NM_003590.4:c.1334G>T NP_003581.1:p.Ser445Ile
XM_006712800.2:c.1301G>T XP_006712863.2:p.Ser434Ile
XM_011511994.1:c.1187G>T XP_011510296.1:p.Ser396Ile
XM_011511995.1:c.1292G>T XP_011510297.1:p.Ser431Ile
XM_011511996.1:c.1142G>T XP_011510298.1:p.Ser381Ile
XM_011511997.1:c.1034G>T XP_011510299.1:p.Ser345Ile
XM_011511994.3:c.1187G>T XP_011510296.1:p.Ser396Ile
XM_011511996.2:c.1142G>T XP_011510298.1:p.Ser381Ile
NM_003590.5:c.1334G>T MANE Select NP_003581.1:p.Ser445Ile
NM_001257198.2:c.1352G>T NP_001244127.1:p.Ser451Ile
NM_001257197.2:c.1136G>T NP_001244126.1:p.Ser379Ile