Canonical Allele Identifier: CA350827697

Gene: CUL3

Linked Data

• dbSNP Id: rs779827356
• MyVariant Identifiers: chr2:g.225368517G>C (hg19) ; chr2:g.224503800G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503800G>C , CM000664.2:g.224503800G>C	GRCh38
NC_000002.11:g.225368517G>C , CM000664.1:g.225368517G>C	GRCh37
NC_000002.10:g.225076761G>C	NCBI36
NG_032169.1:g.86598C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1229C>G MANE Select	ENSP00000264414.4:p.Thr410Arg
ENST00000264414.8:c.1229C>G	ENSP00000264414.4:p.Thr410Arg
ENST00000344951.8:c.1031C>G	ENSP00000343601.4:p.Thr344Arg
ENST00000409096.5:c.1157C>G	ENSP00000387200.1:p.Thr386Arg
ENST00000409777.5:c.1157C>G	ENSP00000386525.1:p.Thr386Arg
ENST00000481135.1:n.525C>G
ENST00000617432.4:c.-48C>G	ENSP00000477851.1:n.-48C>G
NM_001257197.1:c.1031C>G	NP_001244126.1:p.Thr344Arg
NM_001257198.1:c.1247C>G	NP_001244127.1:p.Thr416Arg
NM_003590.4:c.1229C>G	NP_003581.1:p.Thr410Arg
XM_006712800.2:c.1196C>G	XP_006712863.2:p.Thr399Arg
XM_011511994.1:c.1082C>G	XP_011510296.1:p.Thr361Arg
XM_011511995.1:c.1187C>G	XP_011510297.1:p.Thr396Arg
XM_011511996.1:c.1037C>G	XP_011510298.1:p.Thr346Arg
XM_011511997.1:c.929C>G	XP_011510299.1:p.Thr310Arg
XM_011511994.3:c.1082C>G	XP_011510296.1:p.Thr361Arg
XM_011511996.2:c.1037C>G	XP_011510298.1:p.Thr346Arg
NM_003590.5:c.1229C>G MANE Select	NP_003581.1:p.Thr410Arg
NM_001257198.2:c.1247C>G	NP_001244127.1:p.Thr416Arg
NM_001257197.2:c.1031C>G	NP_001244126.1:p.Thr344Arg