Canonical Allele Identifier: CA350827605

Gene: CUL3

Linked Data

• dbSNP Id: rs1214053324
• MyVariant Identifiers: chr2:g.225368494G>C (hg19) ; chr2:g.224503777G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503777G>C , CM000664.2:g.224503777G>C	GRCh38
NC_000002.11:g.225368494G>C , CM000664.1:g.225368494G>C	GRCh37
NC_000002.10:g.225076738G>C	NCBI36
NG_032169.1:g.86621C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1252C>G MANE Select	ENSP00000264414.4:p.Leu418Val
ENST00000264414.8:c.1252C>G	ENSP00000264414.4:p.Leu418Val
ENST00000344951.8:c.1054C>G	ENSP00000343601.4:p.Leu352Val
ENST00000409096.5:c.1180C>G	ENSP00000387200.1:p.Leu394Val
ENST00000409777.5:c.1180C>G	ENSP00000386525.1:p.Leu394Val
ENST00000481135.1:n.548C>G
ENST00000617432.4:c.-25C>G	ENSP00000477851.1:n.-25C>G
NM_001257197.1:c.1054C>G	NP_001244126.1:p.Leu352Val
NM_001257198.1:c.1270C>G	NP_001244127.1:p.Leu424Val
NM_003590.4:c.1252C>G	NP_003581.1:p.Leu418Val
XM_006712800.2:c.1219C>G	XP_006712863.2:p.Leu407Val
XM_011511994.1:c.1105C>G	XP_011510296.1:p.Leu369Val
XM_011511995.1:c.1210C>G	XP_011510297.1:p.Leu404Val
XM_011511996.1:c.1060C>G	XP_011510298.1:p.Leu354Val
XM_011511997.1:c.952C>G	XP_011510299.1:p.Leu318Val
XM_011511994.3:c.1105C>G	XP_011510296.1:p.Leu369Val
XM_011511996.2:c.1060C>G	XP_011510298.1:p.Leu354Val
NM_003590.5:c.1252C>G MANE Select	NP_003581.1:p.Leu418Val
NM_001257198.2:c.1270C>G	NP_001244127.1:p.Leu424Val
NM_001257197.2:c.1054C>G	NP_001244126.1:p.Leu352Val