Canonical Allele Identifier: CA431492710

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368488T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503771T>G , CM000664.2:g.224503771T>G	GRCh38
NC_000002.11:g.225368488T>G , CM000664.1:g.225368488T>G	GRCh37
NC_000002.10:g.225076732T>G	NCBI36
NG_032169.1:g.86627A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1258A>C MANE Select	ENSP00000264414.4:p.Arg420=
ENST00000264414.8:c.1258A>C	ENSP00000264414.4:p.Arg420=
ENST00000344951.8:c.1060A>C	ENSP00000343601.4:p.Arg354=
ENST00000409096.5:c.1186A>C	ENSP00000387200.1:p.Arg396=
ENST00000409777.5:c.1186A>C	ENSP00000386525.1:p.Arg396=
ENST00000481135.1:n.554A>C
ENST00000617432.4:c.-19A>C	ENSP00000477851.1:n.-19A>C
NM_001257197.1:c.1060A>C	NP_001244126.1:p.Arg354=
NM_001257198.1:c.1276A>C	NP_001244127.1:p.Arg426=
NM_003590.4:c.1258A>C	NP_003581.1:p.Arg420=
XM_006712800.2:c.1225A>C	XP_006712863.2:p.Arg409=
XM_011511994.1:c.1111A>C	XP_011510296.1:p.Arg371=
XM_011511995.1:c.1216A>C	XP_011510297.1:p.Arg406=
XM_011511996.1:c.1066A>C	XP_011510298.1:p.Arg356=
XM_011511997.1:c.958A>C	XP_011510299.1:p.Arg320=
XM_011511994.3:c.1111A>C	XP_011510296.1:p.Arg371=
XM_011511996.2:c.1066A>C	XP_011510298.1:p.Arg356=
NM_003590.5:c.1258A>C MANE Select	NP_003581.1:p.Arg420=
NM_001257198.2:c.1276A>C	NP_001244127.1:p.Arg426=
NM_001257197.2:c.1060A>C	NP_001244126.1:p.Arg354=