Canonical Allele Identifier: CA350826976

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368391T>G (hg19) ; chr2:g.224503674T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503674T>G , CM000664.2:g.224503674T>G	GRCh38
NC_000002.11:g.225368391T>G , CM000664.1:g.225368391T>G	GRCh37
NC_000002.10:g.225076635T>G	NCBI36
NG_032169.1:g.86724A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1355A>C MANE Select	ENSP00000264414.4:p.Lys452Thr
ENST00000264414.8:c.1355A>C	ENSP00000264414.4:p.Lys452Thr
ENST00000344951.8:c.1157A>C	ENSP00000343601.4:p.Lys386Thr
ENST00000409096.5:c.1283A>C	ENSP00000387200.1:p.Lys428Thr
ENST00000409777.5:c.1283A>C	ENSP00000386525.1:p.Lys428Thr
ENST00000481135.1:n.651A>C
ENST00000617432.4:c.79-2A>C	ENSP00000477851.1:n.79-2A>C
NM_001257197.1:c.1157A>C	NP_001244126.1:p.Lys386Thr
NM_001257198.1:c.1373A>C	NP_001244127.1:p.Lys458Thr
NM_003590.4:c.1355A>C	NP_003581.1:p.Lys452Thr
XM_006712800.2:c.1322A>C	XP_006712863.2:p.Lys441Thr
XM_011511994.1:c.1208A>C	XP_011510296.1:p.Lys403Thr
XM_011511995.1:c.1313A>C	XP_011510297.1:p.Lys438Thr
XM_011511996.1:c.1163A>C	XP_011510298.1:p.Lys388Thr
XM_011511997.1:c.1055A>C	XP_011510299.1:p.Lys352Thr
XM_011511994.3:c.1208A>C	XP_011510296.1:p.Lys403Thr
XM_011511996.2:c.1163A>C	XP_011510298.1:p.Lys388Thr
NM_003590.5:c.1355A>C MANE Select	NP_003581.1:p.Lys452Thr
NM_001257198.2:c.1373A>C	NP_001244127.1:p.Lys458Thr
NM_001257197.2:c.1157A>C	NP_001244126.1:p.Lys386Thr