Canonical Allele Identifier: CA350827756

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368531T>G (hg19) ; chr2:g.224503814T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503814T>G , CM000664.2:g.224503814T>G	GRCh38
NC_000002.11:g.225368531T>G , CM000664.1:g.225368531T>G	GRCh37
NC_000002.10:g.225076775T>G	NCBI36
NG_032169.1:g.86584A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1215A>C MANE Select	ENSP00000264414.4:p.Glu405Asp
ENST00000264414.8:c.1215A>C	ENSP00000264414.4:p.Glu405Asp
ENST00000344951.8:c.1017A>C	ENSP00000343601.4:p.Glu339Asp
ENST00000409096.5:c.1143A>C	ENSP00000387200.1:p.Glu381Asp
ENST00000409777.5:c.1143A>C	ENSP00000386525.1:p.Glu381Asp
ENST00000481135.1:n.511A>C
ENST00000617432.4:c.-62A>C	ENSP00000477851.1:n.-62A>C
NM_001257197.1:c.1017A>C	NP_001244126.1:p.Glu339Asp
NM_001257198.1:c.1233A>C	NP_001244127.1:p.Glu411Asp
NM_003590.4:c.1215A>C	NP_003581.1:p.Glu405Asp
XM_006712800.2:c.1182A>C	XP_006712863.2:p.Glu394Asp
XM_011511994.1:c.1068A>C	XP_011510296.1:p.Glu356Asp
XM_011511995.1:c.1173A>C	XP_011510297.1:p.Glu391Asp
XM_011511996.1:c.1023A>C	XP_011510298.1:p.Glu341Asp
XM_011511997.1:c.915A>C	XP_011510299.1:p.Glu305Asp
XM_011511994.3:c.1068A>C	XP_011510296.1:p.Glu356Asp
XM_011511996.2:c.1023A>C	XP_011510298.1:p.Glu341Asp
NM_003590.5:c.1215A>C MANE Select	NP_003581.1:p.Glu405Asp
NM_001257198.2:c.1233A>C	NP_001244127.1:p.Glu411Asp
NM_001257197.2:c.1017A>C	NP_001244126.1:p.Glu339Asp