Canonical Allele Identifier: CA350827542

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197232
• MyVariant Identifiers: chr2:g.225368478T>C (hg19) ; chr2:g.224503761T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503761T>C , CM000664.2:g.224503761T>C	GRCh38
NC_000002.11:g.225368478T>C , CM000664.1:g.225368478T>C	GRCh37
NC_000002.10:g.225076722T>C	NCBI36
NG_032169.1:g.86637A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1268A>G MANE Select	ENSP00000264414.4:p.Gln423Arg
ENST00000264414.8:c.1268A>G	ENSP00000264414.4:p.Gln423Arg
ENST00000344951.8:c.1070A>G	ENSP00000343601.4:p.Gln357Arg
ENST00000409096.5:c.1196A>G	ENSP00000387200.1:p.Gln399Arg
ENST00000409777.5:c.1196A>G	ENSP00000386525.1:p.Gln399Arg
ENST00000481135.1:n.564A>G
ENST00000617432.4:c.-9A>G	ENSP00000477851.1:n.-9A>G
NM_001257197.1:c.1070A>G	NP_001244126.1:p.Gln357Arg
NM_001257198.1:c.1286A>G	NP_001244127.1:p.Gln429Arg
NM_003590.4:c.1268A>G	NP_003581.1:p.Gln423Arg
XM_006712800.2:c.1235A>G	XP_006712863.2:p.Gln412Arg
XM_011511994.1:c.1121A>G	XP_011510296.1:p.Gln374Arg
XM_011511995.1:c.1226A>G	XP_011510297.1:p.Gln409Arg
XM_011511996.1:c.1076A>G	XP_011510298.1:p.Gln359Arg
XM_011511997.1:c.968A>G	XP_011510299.1:p.Gln323Arg
XM_011511994.3:c.1121A>G	XP_011510296.1:p.Gln374Arg
XM_011511996.2:c.1076A>G	XP_011510298.1:p.Gln359Arg
NM_003590.5:c.1268A>G MANE Select	NP_003581.1:p.Gln423Arg
NM_001257198.2:c.1286A>G	NP_001244127.1:p.Gln429Arg
NM_001257197.2:c.1070A>G	NP_001244126.1:p.Gln357Arg