Canonical Allele Identifier: CA431492722

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368507A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503790A>G , CM000664.2:g.224503790A>G	GRCh38
NC_000002.11:g.225368507A>G , CM000664.1:g.225368507A>G	GRCh37
NC_000002.10:g.225076751A>G	NCBI36
NG_032169.1:g.86608T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1239T>C MANE Select	ENSP00000264414.4:p.Asp413=
ENST00000264414.8:c.1239T>C	ENSP00000264414.4:p.Asp413=
ENST00000344951.8:c.1041T>C	ENSP00000343601.4:p.Asp347=
ENST00000409096.5:c.1167T>C	ENSP00000387200.1:p.Asp389=
ENST00000409777.5:c.1167T>C	ENSP00000386525.1:p.Asp389=
ENST00000481135.1:n.535T>C
ENST00000617432.4:c.-38T>C	ENSP00000477851.1:n.-38T>C
NM_001257197.1:c.1041T>C	NP_001244126.1:p.Asp347=
NM_001257198.1:c.1257T>C	NP_001244127.1:p.Asp419=
NM_003590.4:c.1239T>C	NP_003581.1:p.Asp413=
XM_006712800.2:c.1206T>C	XP_006712863.2:p.Asp402=
XM_011511994.1:c.1092T>C	XP_011510296.1:p.Asp364=
XM_011511995.1:c.1197T>C	XP_011510297.1:p.Asp399=
XM_011511996.1:c.1047T>C	XP_011510298.1:p.Asp349=
XM_011511997.1:c.939T>C	XP_011510299.1:p.Asp313=
XM_011511994.3:c.1092T>C	XP_011510296.1:p.Asp364=
XM_011511996.2:c.1047T>C	XP_011510298.1:p.Asp349=
NM_003590.5:c.1239T>C MANE Select	NP_003581.1:p.Asp413=
NM_001257198.2:c.1257T>C	NP_001244127.1:p.Asp419=
NM_001257197.2:c.1041T>C	NP_001244126.1:p.Asp347=