Canonical Allele Identifier: CA350827229

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368423G>C (hg19) ; chr2:g.224503706G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503706G>C , CM000664.2:g.224503706G>C	GRCh38
NC_000002.11:g.225368423G>C , CM000664.1:g.225368423G>C	GRCh37
NC_000002.10:g.225076667G>C	NCBI36
NG_032169.1:g.86692C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1323C>G MANE Select	ENSP00000264414.4:p.Leu441=
ENST00000264414.8:c.1323C>G	ENSP00000264414.4:p.Leu441=
ENST00000344951.8:c.1125C>G	ENSP00000343601.4:p.Leu375=
ENST00000409096.5:c.1251C>G	ENSP00000387200.1:p.Leu417=
ENST00000409777.5:c.1251C>G	ENSP00000386525.1:p.Leu417=
ENST00000481135.1:n.619C>G
ENST00000617432.4:c.47C>G	ENSP00000477851.1:p.Ser16Ter
NM_001257197.1:c.1125C>G	NP_001244126.1:p.Leu375=
NM_001257198.1:c.1341C>G	NP_001244127.1:p.Leu447=
NM_003590.4:c.1323C>G	NP_003581.1:p.Leu441=
XM_006712800.2:c.1290C>G	XP_006712863.2:p.Leu430=
XM_011511994.1:c.1176C>G	XP_011510296.1:p.Leu392=
XM_011511995.1:c.1281C>G	XP_011510297.1:p.Leu427=
XM_011511996.1:c.1131C>G	XP_011510298.1:p.Leu377=
XM_011511997.1:c.1023C>G	XP_011510299.1:p.Leu341=
XM_011511994.3:c.1176C>G	XP_011510296.1:p.Leu392=
XM_011511996.2:c.1131C>G	XP_011510298.1:p.Leu377=
NM_003590.5:c.1323C>G MANE Select	NP_003581.1:p.Leu441=
NM_001257198.2:c.1341C>G	NP_001244127.1:p.Leu447=
NM_001257197.2:c.1125C>G	NP_001244126.1:p.Leu375=