Canonical Allele Identifier: CA10602470

Gene: CUL3

Linked Data

• ClinVar Variation Id: 266041
• ClinVar RCV Id: RCV000256456
• dbSNP Id: rs886038765
• MyVariant Identifiers: chr2:g.225368369C>T (hg19) ; chr2:g.224503652C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503652C>T , CM000664.2:g.224503652C>T	GRCh38
NC_000002.11:g.225368369C>T , CM000664.1:g.225368369C>T	GRCh37
NC_000002.10:g.225076613C>T	NCBI36
NG_032169.1:g.86746G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1377G>A MANE Select	ENSP00000264414.4:p.Lys459=
ENST00000264414.8:c.1377G>A	ENSP00000264414.4:p.Lys459=
ENST00000344951.8:c.1179G>A	ENSP00000343601.4:p.Lys393=
ENST00000409096.5:c.1305G>A	ENSP00000387200.1:p.Lys435=
ENST00000409777.5:c.1305G>A	ENSP00000386525.1:p.Lys435=
ENST00000481135.1:n.673G>A
ENST00000617432.4:c.99G>A	ENSP00000477851.1:p.Lys33=
NM_001257197.1:c.1179G>A	NP_001244126.1:p.Lys393=
NM_001257198.1:c.1395G>A	NP_001244127.1:p.Lys465=
NM_003590.4:c.1377G>A	NP_003581.1:p.Lys459=
XM_006712800.2:c.1344G>A	XP_006712863.2:p.Lys448=
XM_011511994.1:c.1230G>A	XP_011510296.1:p.Lys410=
XM_011511995.1:c.1335G>A	XP_011510297.1:p.Lys445=
XM_011511996.1:c.1185G>A	XP_011510298.1:p.Lys395=
XM_011511997.1:c.1077G>A	XP_011510299.1:p.Lys359=
XM_011511994.3:c.1230G>A	XP_011510296.1:p.Lys410=
XM_011511996.2:c.1185G>A	XP_011510298.1:p.Lys395=
NM_003590.5:c.1377G>A MANE Select	NP_003581.1:p.Lys459=
NM_001257198.2:c.1395G>A	NP_001244127.1:p.Lys465=
NM_001257197.2:c.1179G>A	NP_001244126.1:p.Lys393=