Canonical Allele Identifier: CA350827549

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368481A>C (hg19) ; chr2:g.224503764A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503764A>C , CM000664.2:g.224503764A>C	GRCh38
NC_000002.11:g.225368481A>C , CM000664.1:g.225368481A>C	GRCh37
NC_000002.10:g.225076725A>C	NCBI36
NG_032169.1:g.86634T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1265T>G MANE Select	ENSP00000264414.4:p.Met422Arg
ENST00000264414.8:c.1265T>G	ENSP00000264414.4:p.Met422Arg
ENST00000344951.8:c.1067T>G	ENSP00000343601.4:p.Met356Arg
ENST00000409096.5:c.1193T>G	ENSP00000387200.1:p.Met398Arg
ENST00000409777.5:c.1193T>G	ENSP00000386525.1:p.Met398Arg
ENST00000481135.1:n.561T>G
ENST00000617432.4:c.-12T>G	ENSP00000477851.1:n.-12T>G
NM_001257197.1:c.1067T>G	NP_001244126.1:p.Met356Arg
NM_001257198.1:c.1283T>G	NP_001244127.1:p.Met428Arg
NM_003590.4:c.1265T>G	NP_003581.1:p.Met422Arg
XM_006712800.2:c.1232T>G	XP_006712863.2:p.Met411Arg
XM_011511994.1:c.1118T>G	XP_011510296.1:p.Met373Arg
XM_011511995.1:c.1223T>G	XP_011510297.1:p.Met408Arg
XM_011511996.1:c.1073T>G	XP_011510298.1:p.Met358Arg
XM_011511997.1:c.965T>G	XP_011510299.1:p.Met322Arg
XM_011511994.3:c.1118T>G	XP_011510296.1:p.Met373Arg
XM_011511996.2:c.1073T>G	XP_011510298.1:p.Met358Arg
NM_003590.5:c.1265T>G MANE Select	NP_003581.1:p.Met422Arg
NM_001257198.2:c.1283T>G	NP_001244127.1:p.Met428Arg
NM_001257197.2:c.1067T>G	NP_001244126.1:p.Met356Arg