Canonical Allele Identifier: CA350831110

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224513537G>C , CM000664.2:g.224513537G>C	GRCh38
NC_000002.11:g.225378254G>C , CM000664.1:g.225378254G>C	GRCh37
NC_000002.10:g.225086498G>C	NCBI36
NG_032169.1:g.76861C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003590.5:c.641C>G MANE Select	NP_003581.1:p.Ala214Gly
ENST00000264414.9:c.641C>G MANE Select	ENSP00000264414.4:p.Ala214Gly
NM_001257197.1:c.443C>G	NP_001244126.1:p.Ala148Gly
NM_001257197.2:c.443C>G	NP_001244126.1:p.Ala148Gly
NM_001257198.1:c.659C>G	NP_001244127.1:p.Ala220Gly
NM_001257198.2:c.659C>G	NP_001244127.1:p.Ala220Gly
NM_003590.4:c.641C>G	NP_003581.1:p.Ala214Gly
ENST00000264414.8:c.641C>G	ENSP00000264414.4:p.Ala214Gly
ENST00000344951.8:c.443C>G	ENSP00000343601.4:p.Ala148Gly
ENST00000409096.5:c.569C>G	ENSP00000387200.1:p.Ala190Gly
ENST00000409777.5:c.569C>G	ENSP00000386525.1:p.Ala190Gly
ENST00000541548.5:n.377C>G
XM_006712800.2:c.608C>G	XP_006712863.2:p.Ala203Gly
XM_011511994.1:c.494C>G	XP_011510296.1:p.Ala165Gly
XM_011511994.3:c.494C>G	XP_011510296.1:p.Ala165Gly
XM_011511995.1:c.599C>G	XP_011510297.1:p.Ala200Gly
XM_011511996.1:c.449C>G	XP_011510298.1:p.Ala150Gly
XM_011511996.2:c.449C>G	XP_011510298.1:p.Ala150Gly
XM_011511997.1:c.341C>G	XP_011510299.1:p.Ala114Gly