Canonical Allele Identifier: CA350827519

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197197
• COSMIC: COSM3938951
• MyVariant Identifiers: chr2:g.225368470C>G (hg19) ; chr2:g.224503753C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503753C>G , CM000664.2:g.224503753C>G	GRCh38
NC_000002.11:g.225368470C>G , CM000664.1:g.225368470C>G	GRCh37
NC_000002.10:g.225076714C>G	NCBI36
NG_032169.1:g.86645G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1276G>C MANE Select	ENSP00000264414.4:p.Asp426His
ENST00000264414.8:c.1276G>C	ENSP00000264414.4:p.Asp426His
ENST00000344951.8:c.1078G>C	ENSP00000343601.4:p.Asp360His
ENST00000409096.5:c.1204G>C	ENSP00000387200.1:p.Asp402His
ENST00000409777.5:c.1204G>C	ENSP00000386525.1:p.Asp402His
ENST00000481135.1:n.572G>C
ENST00000617432.4:c.-1G>C	ENSP00000477851.1:n.-1G>C
NM_001257197.1:c.1078G>C	NP_001244126.1:p.Asp360His
NM_001257198.1:c.1294G>C	NP_001244127.1:p.Asp432His
NM_003590.4:c.1276G>C	NP_003581.1:p.Asp426His
XM_006712800.2:c.1243G>C	XP_006712863.2:p.Asp415His
XM_011511994.1:c.1129G>C	XP_011510296.1:p.Asp377His
XM_011511995.1:c.1234G>C	XP_011510297.1:p.Asp412His
XM_011511996.1:c.1084G>C	XP_011510298.1:p.Asp362His
XM_011511997.1:c.976G>C	XP_011510299.1:p.Asp326His
XM_011511994.3:c.1129G>C	XP_011510296.1:p.Asp377His
XM_011511996.2:c.1084G>C	XP_011510298.1:p.Asp362His
NM_003590.5:c.1276G>C MANE Select	NP_003581.1:p.Asp426His
NM_001257198.2:c.1294G>C	NP_001244127.1:p.Asp432His
NM_001257197.2:c.1078G>C	NP_001244126.1:p.Asp360His