Canonical Allele Identifier: CA350827637

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368502G>A (hg19) ; chr2:g.224503785G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503785G>A , CM000664.2:g.224503785G>A	GRCh38
NC_000002.11:g.225368502G>A , CM000664.1:g.225368502G>A	GRCh37
NC_000002.10:g.225076746G>A	NCBI36
NG_032169.1:g.86613C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1244C>T MANE Select	ENSP00000264414.4:p.Ala415Val
ENST00000264414.8:c.1244C>T	ENSP00000264414.4:p.Ala415Val
ENST00000344951.8:c.1046C>T	ENSP00000343601.4:p.Ala349Val
ENST00000409096.5:c.1172C>T	ENSP00000387200.1:p.Ala391Val
ENST00000409777.5:c.1172C>T	ENSP00000386525.1:p.Ala391Val
ENST00000481135.1:n.540C>T
ENST00000617432.4:c.-33C>T	ENSP00000477851.1:n.-33C>T
NM_001257197.1:c.1046C>T	NP_001244126.1:p.Ala349Val
NM_001257198.1:c.1262C>T	NP_001244127.1:p.Ala421Val
NM_003590.4:c.1244C>T	NP_003581.1:p.Ala415Val
XM_006712800.2:c.1211C>T	XP_006712863.2:p.Ala404Val
XM_011511994.1:c.1097C>T	XP_011510296.1:p.Ala366Val
XM_011511995.1:c.1202C>T	XP_011510297.1:p.Ala401Val
XM_011511996.1:c.1052C>T	XP_011510298.1:p.Ala351Val
XM_011511997.1:c.944C>T	XP_011510299.1:p.Ala315Val
XM_011511994.3:c.1097C>T	XP_011510296.1:p.Ala366Val
XM_011511996.2:c.1052C>T	XP_011510298.1:p.Ala351Val
NM_003590.5:c.1244C>T MANE Select	NP_003581.1:p.Ala415Val
NM_001257198.2:c.1262C>T	NP_001244127.1:p.Ala421Val
NM_001257197.2:c.1046C>T	NP_001244126.1:p.Ala349Val