Canonical Allele Identifier: CA350827593

Gene: CUL3

Linked Data

• gnomAD v4: 2-224503774-A-G
• MyVariant Identifiers: chr2:g.225368491A>G (hg19) ; chr2:g.224503774A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1255T>C MANE Select	ENSP00000264414.4:p.Phe419Leu
ENST00000264414.8:c.1255T>C	ENSP00000264414.4:p.Phe419Leu
ENST00000344951.8:c.1057T>C	ENSP00000343601.4:p.Phe353Leu
ENST00000409096.5:c.1183T>C	ENSP00000387200.1:p.Phe395Leu
ENST00000409777.5:c.1183T>C	ENSP00000386525.1:p.Phe395Leu
ENST00000481135.1:n.551T>C
ENST00000617432.4:c.-22T>C	ENSP00000477851.1:n.-22T>C
NM_001257197.1:c.1057T>C	NP_001244126.1:p.Phe353Leu
NM_001257198.1:c.1273T>C	NP_001244127.1:p.Phe425Leu
NM_003590.4:c.1255T>C	NP_003581.1:p.Phe419Leu
XM_006712800.2:c.1222T>C	XP_006712863.2:p.Phe408Leu
XM_011511994.1:c.1108T>C	XP_011510296.1:p.Phe370Leu
XM_011511995.1:c.1213T>C	XP_011510297.1:p.Phe405Leu
XM_011511996.1:c.1063T>C	XP_011510298.1:p.Phe355Leu
XM_011511997.1:c.955T>C	XP_011510299.1:p.Phe319Leu
XM_011511994.3:c.1108T>C	XP_011510296.1:p.Phe370Leu
XM_011511996.2:c.1063T>C	XP_011510298.1:p.Phe355Leu
NM_003590.5:c.1255T>C MANE Select	NP_003581.1:p.Phe419Leu
NM_001257198.2:c.1273T>C	NP_001244127.1:p.Phe425Leu
NM_001257197.2:c.1057T>C	NP_001244126.1:p.Phe353Leu