Canonical Allele Identifier: CA431492565

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368381T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503664T>G , CM000664.2:g.224503664T>G	GRCh38
NC_000002.11:g.225368381T>G , CM000664.1:g.225368381T>G	GRCh37
NC_000002.10:g.225076625T>G	NCBI36
NG_032169.1:g.86734A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1365A>C MANE Select	ENSP00000264414.4:p.Ile455=
ENST00000264414.8:c.1365A>C	ENSP00000264414.4:p.Ile455=
ENST00000344951.8:c.1167A>C	ENSP00000343601.4:p.Ile389=
ENST00000409096.5:c.1293A>C	ENSP00000387200.1:p.Ile431=
ENST00000409777.5:c.1293A>C	ENSP00000386525.1:p.Ile431=
ENST00000481135.1:n.661A>C
ENST00000617432.4:c.87A>C	ENSP00000477851.1:p.Ile29=
NM_001257197.1:c.1167A>C	NP_001244126.1:p.Ile389=
NM_001257198.1:c.1383A>C	NP_001244127.1:p.Ile461=
NM_003590.4:c.1365A>C	NP_003581.1:p.Ile455=
XM_006712800.2:c.1332A>C	XP_006712863.2:p.Ile444=
XM_011511994.1:c.1218A>C	XP_011510296.1:p.Ile406=
XM_011511995.1:c.1323A>C	XP_011510297.1:p.Ile441=
XM_011511996.1:c.1173A>C	XP_011510298.1:p.Ile391=
XM_011511997.1:c.1065A>C	XP_011510299.1:p.Ile355=
XM_011511994.3:c.1218A>C	XP_011510296.1:p.Ile406=
XM_011511996.2:c.1173A>C	XP_011510298.1:p.Ile391=
NM_003590.5:c.1365A>C MANE Select	NP_003581.1:p.Ile455=
NM_001257198.2:c.1383A>C	NP_001244127.1:p.Ile461=
NM_001257197.2:c.1167A>C	NP_001244126.1:p.Ile389=