Canonical Allele Identifier: CA350827564

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197291
• MyVariant Identifiers: chr2:g.225368485A>T (hg19) ; chr2:g.224503768A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503768A>T , CM000664.2:g.224503768A>T	GRCh38
NC_000002.11:g.225368485A>T , CM000664.1:g.225368485A>T	GRCh37
NC_000002.10:g.225076729A>T	NCBI36
NG_032169.1:g.86630T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1261T>A MANE Select	ENSP00000264414.4:p.Phe421Ile
ENST00000264414.8:c.1261T>A	ENSP00000264414.4:p.Phe421Ile
ENST00000344951.8:c.1063T>A	ENSP00000343601.4:p.Phe355Ile
ENST00000409096.5:c.1189T>A	ENSP00000387200.1:p.Phe397Ile
ENST00000409777.5:c.1189T>A	ENSP00000386525.1:p.Phe397Ile
ENST00000481135.1:n.557T>A
ENST00000617432.4:c.-16T>A	ENSP00000477851.1:n.-16T>A
NM_001257197.1:c.1063T>A	NP_001244126.1:p.Phe355Ile
NM_001257198.1:c.1279T>A	NP_001244127.1:p.Phe427Ile
NM_003590.4:c.1261T>A	NP_003581.1:p.Phe421Ile
XM_006712800.2:c.1228T>A	XP_006712863.2:p.Phe410Ile
XM_011511994.1:c.1114T>A	XP_011510296.1:p.Phe372Ile
XM_011511995.1:c.1219T>A	XP_011510297.1:p.Phe407Ile
XM_011511996.1:c.1069T>A	XP_011510298.1:p.Phe357Ile
XM_011511997.1:c.961T>A	XP_011510299.1:p.Phe321Ile
XM_011511994.3:c.1114T>A	XP_011510296.1:p.Phe372Ile
XM_011511996.2:c.1069T>A	XP_011510298.1:p.Phe357Ile
NM_003590.5:c.1261T>A MANE Select	NP_003581.1:p.Phe421Ile
NM_001257198.2:c.1279T>A	NP_001244127.1:p.Phe427Ile
NM_001257197.2:c.1063T>A	NP_001244126.1:p.Phe355Ile