Canonical Allele Identifier: CA350827354

Gene: CUL3

Linked Data

• dbSNP Id: rs1178533914
• MyVariant Identifiers: chr2:g.225368441G>C (hg19) ; chr2:g.224503724G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503724G>C , CM000664.2:g.224503724G>C	GRCh38
NC_000002.11:g.225368441G>C , CM000664.1:g.225368441G>C	GRCh37
NC_000002.10:g.225076685G>C	NCBI36
NG_032169.1:g.86674C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1305C>G MANE Select	ENSP00000264414.4:p.His435Gln
ENST00000264414.8:c.1305C>G	ENSP00000264414.4:p.His435Gln
ENST00000344951.8:c.1107C>G	ENSP00000343601.4:p.His369Gln
ENST00000409096.5:c.1233C>G	ENSP00000387200.1:p.His411Gln
ENST00000409777.5:c.1233C>G	ENSP00000386525.1:p.His411Gln
ENST00000481135.1:n.601C>G
ENST00000617432.4:c.29C>G	ENSP00000477851.1:p.Thr10Ser
NM_001257197.1:c.1107C>G	NP_001244126.1:p.His369Gln
NM_001257198.1:c.1323C>G	NP_001244127.1:p.His441Gln
NM_003590.4:c.1305C>G	NP_003581.1:p.His435Gln
XM_006712800.2:c.1272C>G	XP_006712863.2:p.His424Gln
XM_011511994.1:c.1158C>G	XP_011510296.1:p.His386Gln
XM_011511995.1:c.1263C>G	XP_011510297.1:p.His421Gln
XM_011511996.1:c.1113C>G	XP_011510298.1:p.His371Gln
XM_011511997.1:c.1005C>G	XP_011510299.1:p.His335Gln
XM_011511994.3:c.1158C>G	XP_011510296.1:p.His386Gln
XM_011511996.2:c.1113C>G	XP_011510298.1:p.His371Gln
NM_003590.5:c.1305C>G MANE Select	NP_003581.1:p.His435Gln
NM_001257198.2:c.1323C>G	NP_001244127.1:p.His441Gln
NM_001257197.2:c.1107C>G	NP_001244126.1:p.His369Gln