Canonical Allele Identifier: CA2140015

Gene: CUL3

Linked Data

• dbSNP Id: rs764528056
• ExAC: 2:225368381 T / C
• gnomAD v2: 2-225368381-T-C
• gnomAD v4: 2-224503664-T-C
• MyVariant Identifiers: chr2:g.225368381T>C (hg19) ; chr2:g.224503664T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503664T>C , CM000664.2:g.224503664T>C	GRCh38
NC_000002.11:g.225368381T>C , CM000664.1:g.225368381T>C	GRCh37
NC_000002.10:g.225076625T>C	NCBI36
NG_032169.1:g.86734A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1365A>G MANE Select	ENSP00000264414.4:p.Ile455Met
ENST00000264414.8:c.1365A>G	ENSP00000264414.4:p.Ile455Met
ENST00000344951.8:c.1167A>G	ENSP00000343601.4:p.Ile389Met
ENST00000409096.5:c.1293A>G	ENSP00000387200.1:p.Ile431Met
ENST00000409777.5:c.1293A>G	ENSP00000386525.1:p.Ile431Met
ENST00000481135.1:n.661A>G
ENST00000617432.4:c.87A>G	ENSP00000477851.1:p.Ile29Met
NM_001257197.1:c.1167A>G	NP_001244126.1:p.Ile389Met
NM_001257198.1:c.1383A>G	NP_001244127.1:p.Ile461Met
NM_003590.4:c.1365A>G	NP_003581.1:p.Ile455Met
XM_006712800.2:c.1332A>G	XP_006712863.2:p.Ile444Met
XM_011511994.1:c.1218A>G	XP_011510296.1:p.Ile406Met
XM_011511995.1:c.1323A>G	XP_011510297.1:p.Ile441Met
XM_011511996.1:c.1173A>G	XP_011510298.1:p.Ile391Met
XM_011511997.1:c.1065A>G	XP_011510299.1:p.Ile355Met
XM_011511994.3:c.1218A>G	XP_011510296.1:p.Ile406Met
XM_011511996.2:c.1173A>G	XP_011510298.1:p.Ile391Met
NM_003590.5:c.1365A>G MANE Select	NP_003581.1:p.Ile455Met
NM_001257198.2:c.1383A>G	NP_001244127.1:p.Ile461Met
NM_001257197.2:c.1167A>G	NP_001244126.1:p.Ile389Met