Canonical Allele Identifier: CA350827439

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368454T>C (hg19) ; chr2:g.224503737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503737T>C , CM000664.2:g.224503737T>C	GRCh38
NC_000002.11:g.225368454T>C , CM000664.1:g.225368454T>C	GRCh37
NC_000002.10:g.225076698T>C	NCBI36
NG_032169.1:g.86661A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1292A>G MANE Select	ENSP00000264414.4:p.Tyr431Cys
ENST00000264414.8:c.1292A>G	ENSP00000264414.4:p.Tyr431Cys
ENST00000344951.8:c.1094A>G	ENSP00000343601.4:p.Tyr365Cys
ENST00000409096.5:c.1220A>G	ENSP00000387200.1:p.Tyr407Cys
ENST00000409777.5:c.1220A>G	ENSP00000386525.1:p.Tyr407Cys
ENST00000481135.1:n.588A>G
ENST00000617432.4:c.16A>G	ENSP00000477851.1:p.Ile6Val
NM_001257197.1:c.1094A>G	NP_001244126.1:p.Tyr365Cys
NM_001257198.1:c.1310A>G	NP_001244127.1:p.Tyr437Cys
NM_003590.4:c.1292A>G	NP_003581.1:p.Tyr431Cys
XM_006712800.2:c.1259A>G	XP_006712863.2:p.Tyr420Cys
XM_011511994.1:c.1145A>G	XP_011510296.1:p.Tyr382Cys
XM_011511995.1:c.1250A>G	XP_011510297.1:p.Tyr417Cys
XM_011511996.1:c.1100A>G	XP_011510298.1:p.Tyr367Cys
XM_011511997.1:c.992A>G	XP_011510299.1:p.Tyr331Cys
XM_011511994.3:c.1145A>G	XP_011510296.1:p.Tyr382Cys
XM_011511996.2:c.1100A>G	XP_011510298.1:p.Tyr367Cys
NM_003590.5:c.1292A>G MANE Select	NP_003581.1:p.Tyr431Cys
NM_001257198.2:c.1310A>G	NP_001244127.1:p.Tyr437Cys
NM_001257197.2:c.1094A>G	NP_001244126.1:p.Tyr365Cys