Canonical Allele Identifier: CA350826970

Gene: CUL3

Linked Data

• dbSNP Id: rs1692484997
• MyVariant Identifiers: chr2:g.225368390T>C (hg19) ; chr2:g.224503673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503673T>C , CM000664.2:g.224503673T>C	GRCh38
NC_000002.11:g.225368390T>C , CM000664.1:g.225368390T>C	GRCh37
NC_000002.10:g.225076634T>C	NCBI36
NG_032169.1:g.86725A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1356A>G MANE Select	ENSP00000264414.4:p.Lys452=
ENST00000264414.8:c.1356A>G	ENSP00000264414.4:p.Lys452=
ENST00000344951.8:c.1158A>G	ENSP00000343601.4:p.Lys386=
ENST00000409096.5:c.1284A>G	ENSP00000387200.1:p.Lys428=
ENST00000409777.5:c.1284A>G	ENSP00000386525.1:p.Lys428=
ENST00000481135.1:n.652A>G
ENST00000617432.4:c.79-1A>G	ENSP00000477851.1:n.79-1A>G
NM_001257197.1:c.1158A>G	NP_001244126.1:p.Lys386=
NM_001257198.1:c.1374A>G	NP_001244127.1:p.Lys458=
NM_003590.4:c.1356A>G	NP_003581.1:p.Lys452=
XM_006712800.2:c.1323A>G	XP_006712863.2:p.Lys441=
XM_011511994.1:c.1209A>G	XP_011510296.1:p.Lys403=
XM_011511995.1:c.1314A>G	XP_011510297.1:p.Lys438=
XM_011511996.1:c.1164A>G	XP_011510298.1:p.Lys388=
XM_011511997.1:c.1056A>G	XP_011510299.1:p.Lys352=
XM_011511994.3:c.1209A>G	XP_011510296.1:p.Lys403=
XM_011511996.2:c.1164A>G	XP_011510298.1:p.Lys388=
NM_003590.5:c.1356A>G MANE Select	NP_003581.1:p.Lys452=
NM_001257198.2:c.1374A>G	NP_001244127.1:p.Lys458=
NM_001257197.2:c.1158A>G	NP_001244126.1:p.Lys386=