Canonical Allele Identifier: CA350826924

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368382A>G (hg19) ; chr2:g.224503665A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503665A>G , CM000664.2:g.224503665A>G	GRCh38
NC_000002.11:g.225368382A>G , CM000664.1:g.225368382A>G	GRCh37
NC_000002.10:g.225076626A>G	NCBI36
NG_032169.1:g.86733T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1364T>C MANE Select	ENSP00000264414.4:p.Ile455Thr
ENST00000264414.8:c.1364T>C	ENSP00000264414.4:p.Ile455Thr
ENST00000344951.8:c.1166T>C	ENSP00000343601.4:p.Ile389Thr
ENST00000409096.5:c.1292T>C	ENSP00000387200.1:p.Ile431Thr
ENST00000409777.5:c.1292T>C	ENSP00000386525.1:p.Ile431Thr
ENST00000481135.1:n.660T>C
ENST00000617432.4:c.86T>C	ENSP00000477851.1:p.Ile29Thr
NM_001257197.1:c.1166T>C	NP_001244126.1:p.Ile389Thr
NM_001257198.1:c.1382T>C	NP_001244127.1:p.Ile461Thr
NM_003590.4:c.1364T>C	NP_003581.1:p.Ile455Thr
XM_006712800.2:c.1331T>C	XP_006712863.2:p.Ile444Thr
XM_011511994.1:c.1217T>C	XP_011510296.1:p.Ile406Thr
XM_011511995.1:c.1322T>C	XP_011510297.1:p.Ile441Thr
XM_011511996.1:c.1172T>C	XP_011510298.1:p.Ile391Thr
XM_011511997.1:c.1064T>C	XP_011510299.1:p.Ile355Thr
XM_011511994.3:c.1217T>C	XP_011510296.1:p.Ile406Thr
XM_011511996.2:c.1172T>C	XP_011510298.1:p.Ile391Thr
NM_003590.5:c.1364T>C MANE Select	NP_003581.1:p.Ile455Thr
NM_001257198.2:c.1382T>C	NP_001244127.1:p.Ile461Thr
NM_001257197.2:c.1166T>C	NP_001244126.1:p.Ile389Thr