Canonical Allele Identifier: CA350827561

Gene: CUL3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1261T>G MANE Select	ENSP00000264414.4:p.Phe421Val
ENST00000264414.8:c.1261T>G	ENSP00000264414.4:p.Phe421Val
ENST00000344951.8:c.1063T>G	ENSP00000343601.4:p.Phe355Val
ENST00000409096.5:c.1189T>G	ENSP00000387200.1:p.Phe397Val
ENST00000409777.5:c.1189T>G	ENSP00000386525.1:p.Phe397Val
ENST00000481135.1:n.557T>G
ENST00000617432.4:c.-16T>G	ENSP00000477851.1:n.-16T>G
NM_001257197.1:c.1063T>G	NP_001244126.1:p.Phe355Val
NM_001257198.1:c.1279T>G	NP_001244127.1:p.Phe427Val
NM_003590.4:c.1261T>G	NP_003581.1:p.Phe421Val
XM_006712800.2:c.1228T>G	XP_006712863.2:p.Phe410Val
XM_011511994.1:c.1114T>G	XP_011510296.1:p.Phe372Val
XM_011511995.1:c.1219T>G	XP_011510297.1:p.Phe407Val
XM_011511996.1:c.1069T>G	XP_011510298.1:p.Phe357Val
XM_011511997.1:c.961T>G	XP_011510299.1:p.Phe321Val
XM_011511994.3:c.1114T>G	XP_011510296.1:p.Phe372Val
XM_011511996.2:c.1069T>G	XP_011510298.1:p.Phe357Val
NM_003590.5:c.1261T>G MANE Select	NP_003581.1:p.Phe421Val
NM_001257198.2:c.1279T>G	NP_001244127.1:p.Phe427Val
NM_001257197.2:c.1063T>G	NP_001244126.1:p.Phe355Val