Canonical Allele Identifier: CA350827591

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368491A>C (hg19) ; chr2:g.224503774A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503774A>C , CM000664.2:g.224503774A>C	GRCh38
NC_000002.11:g.225368491A>C , CM000664.1:g.225368491A>C	GRCh37
NC_000002.10:g.225076735A>C	NCBI36
NG_032169.1:g.86624T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1255T>G MANE Select	ENSP00000264414.4:p.Phe419Val
ENST00000264414.8:c.1255T>G	ENSP00000264414.4:p.Phe419Val
ENST00000344951.8:c.1057T>G	ENSP00000343601.4:p.Phe353Val
ENST00000409096.5:c.1183T>G	ENSP00000387200.1:p.Phe395Val
ENST00000409777.5:c.1183T>G	ENSP00000386525.1:p.Phe395Val
ENST00000481135.1:n.551T>G
ENST00000617432.4:c.-22T>G	ENSP00000477851.1:n.-22T>G
NM_001257197.1:c.1057T>G	NP_001244126.1:p.Phe353Val
NM_001257198.1:c.1273T>G	NP_001244127.1:p.Phe425Val
NM_003590.4:c.1255T>G	NP_003581.1:p.Phe419Val
XM_006712800.2:c.1222T>G	XP_006712863.2:p.Phe408Val
XM_011511994.1:c.1108T>G	XP_011510296.1:p.Phe370Val
XM_011511995.1:c.1213T>G	XP_011510297.1:p.Phe405Val
XM_011511996.1:c.1063T>G	XP_011510298.1:p.Phe355Val
XM_011511997.1:c.955T>G	XP_011510299.1:p.Phe319Val
XM_011511994.3:c.1108T>G	XP_011510296.1:p.Phe370Val
XM_011511996.2:c.1063T>G	XP_011510298.1:p.Phe355Val
NM_003590.5:c.1255T>G MANE Select	NP_003581.1:p.Phe419Val
NM_001257198.2:c.1273T>G	NP_001244127.1:p.Phe425Val
NM_001257197.2:c.1057T>G	NP_001244126.1:p.Phe353Val