Canonical Allele Identifier: CA350826929

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368383T>G (hg19) ; chr2:g.224503666T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503666T>G , CM000664.2:g.224503666T>G	GRCh38
NC_000002.11:g.225368383T>G , CM000664.1:g.225368383T>G	GRCh37
NC_000002.10:g.225076627T>G	NCBI36
NG_032169.1:g.86732A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1363A>C MANE Select	ENSP00000264414.4:p.Ile455Leu
ENST00000264414.8:c.1363A>C	ENSP00000264414.4:p.Ile455Leu
ENST00000344951.8:c.1165A>C	ENSP00000343601.4:p.Ile389Leu
ENST00000409096.5:c.1291A>C	ENSP00000387200.1:p.Ile431Leu
ENST00000409777.5:c.1291A>C	ENSP00000386525.1:p.Ile431Leu
ENST00000481135.1:n.659A>C
ENST00000617432.4:c.85A>C	ENSP00000477851.1:p.Ile29Leu
NM_001257197.1:c.1165A>C	NP_001244126.1:p.Ile389Leu
NM_001257198.1:c.1381A>C	NP_001244127.1:p.Ile461Leu
NM_003590.4:c.1363A>C	NP_003581.1:p.Ile455Leu
XM_006712800.2:c.1330A>C	XP_006712863.2:p.Ile444Leu
XM_011511994.1:c.1216A>C	XP_011510296.1:p.Ile406Leu
XM_011511995.1:c.1321A>C	XP_011510297.1:p.Ile441Leu
XM_011511996.1:c.1171A>C	XP_011510298.1:p.Ile391Leu
XM_011511997.1:c.1063A>C	XP_011510299.1:p.Ile355Leu
XM_011511994.3:c.1216A>C	XP_011510296.1:p.Ile406Leu
XM_011511996.2:c.1171A>C	XP_011510298.1:p.Ile391Leu
NM_003590.5:c.1363A>C MANE Select	NP_003581.1:p.Ile455Leu
NM_001257198.2:c.1381A>C	NP_001244127.1:p.Ile461Leu
NM_001257197.2:c.1165A>C	NP_001244126.1:p.Ile389Leu