Canonical Allele Identifier: CA350827526
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503755T>G , CM000664.2:g.224503755T>G GRCh38
NC_000002.11:g.225368472T>G , CM000664.1:g.225368472T>G GRCh37
NC_000002.10:g.225076716T>G NCBI36
NG_032169.1:g.86643A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264414.9:c.1274A>C MANE Select ENSP00000264414.4:p.Lys425Thr
ENST00000264414.8:c.1274A>C ENSP00000264414.4:p.Lys425Thr
ENST00000344951.8:c.1076A>C ENSP00000343601.4:p.Lys359Thr
ENST00000409096.5:c.1202A>C ENSP00000387200.1:p.Lys401Thr
ENST00000409777.5:c.1202A>C ENSP00000386525.1:p.Lys401Thr
ENST00000481135.1:n.570A>C
ENST00000617432.4:c.-3A>C ENSP00000477851.1:n.-3A>C
NM_001257197.1:c.1076A>C NP_001244126.1:p.Lys359Thr
NM_001257198.1:c.1292A>C NP_001244127.1:p.Lys431Thr
NM_003590.4:c.1274A>C NP_003581.1:p.Lys425Thr
XM_006712800.2:c.1241A>C XP_006712863.2:p.Lys414Thr
XM_011511994.1:c.1127A>C XP_011510296.1:p.Lys376Thr
XM_011511995.1:c.1232A>C XP_011510297.1:p.Lys411Thr
XM_011511996.1:c.1082A>C XP_011510298.1:p.Lys361Thr
XM_011511997.1:c.974A>C XP_011510299.1:p.Lys325Thr
XM_011511994.3:c.1127A>C XP_011510296.1:p.Lys376Thr
XM_011511996.2:c.1082A>C XP_011510298.1:p.Lys361Thr
NM_003590.5:c.1274A>C MANE Select NP_003581.1:p.Lys425Thr
NM_001257198.2:c.1292A>C NP_001244127.1:p.Lys431Thr
NM_001257197.2:c.1076A>C NP_001244126.1:p.Lys359Thr