Canonical Allele Identifier: CA350827307

Gene: CUL3

Linked Data

• dbSNP Id: rs2106196896
• MyVariant Identifiers: chr2:g.225368433C>G (hg19) ; chr2:g.224503716C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503716C>G , CM000664.2:g.224503716C>G	GRCh38
NC_000002.11:g.225368433C>G , CM000664.1:g.225368433C>G	GRCh37
NC_000002.10:g.225076677C>G	NCBI36
NG_032169.1:g.86682G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1313G>C MANE Select	ENSP00000264414.4:p.Arg438Thr
ENST00000264414.8:c.1313G>C	ENSP00000264414.4:p.Arg438Thr
ENST00000344951.8:c.1115G>C	ENSP00000343601.4:p.Arg372Thr
ENST00000409096.5:c.1241G>C	ENSP00000387200.1:p.Arg414Thr
ENST00000409777.5:c.1241G>C	ENSP00000386525.1:p.Arg414Thr
ENST00000481135.1:n.609G>C
ENST00000617432.4:c.37G>C	ENSP00000477851.1:p.Gly13Arg
NM_001257197.1:c.1115G>C	NP_001244126.1:p.Arg372Thr
NM_001257198.1:c.1331G>C	NP_001244127.1:p.Arg444Thr
NM_003590.4:c.1313G>C	NP_003581.1:p.Arg438Thr
XM_006712800.2:c.1280G>C	XP_006712863.2:p.Arg427Thr
XM_011511994.1:c.1166G>C	XP_011510296.1:p.Arg389Thr
XM_011511995.1:c.1271G>C	XP_011510297.1:p.Arg424Thr
XM_011511996.1:c.1121G>C	XP_011510298.1:p.Arg374Thr
XM_011511997.1:c.1013G>C	XP_011510299.1:p.Arg338Thr
XM_011511994.3:c.1166G>C	XP_011510296.1:p.Arg389Thr
XM_011511996.2:c.1121G>C	XP_011510298.1:p.Arg374Thr
NM_003590.5:c.1313G>C MANE Select	NP_003581.1:p.Arg438Thr
NM_001257198.2:c.1331G>C	NP_001244127.1:p.Arg444Thr
NM_001257197.2:c.1115G>C	NP_001244126.1:p.Arg372Thr