Canonical Allele Identifier: CA350827562

Gene: CUL3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1261T>C MANE Select	ENSP00000264414.4:p.Phe421Leu
ENST00000264414.8:c.1261T>C	ENSP00000264414.4:p.Phe421Leu
ENST00000344951.8:c.1063T>C	ENSP00000343601.4:p.Phe355Leu
ENST00000409096.5:c.1189T>C	ENSP00000387200.1:p.Phe397Leu
ENST00000409777.5:c.1189T>C	ENSP00000386525.1:p.Phe397Leu
ENST00000481135.1:n.557T>C
ENST00000617432.4:c.-16T>C	ENSP00000477851.1:n.-16T>C
NM_001257197.1:c.1063T>C	NP_001244126.1:p.Phe355Leu
NM_001257198.1:c.1279T>C	NP_001244127.1:p.Phe427Leu
NM_003590.4:c.1261T>C	NP_003581.1:p.Phe421Leu
XM_006712800.2:c.1228T>C	XP_006712863.2:p.Phe410Leu
XM_011511994.1:c.1114T>C	XP_011510296.1:p.Phe372Leu
XM_011511995.1:c.1219T>C	XP_011510297.1:p.Phe407Leu
XM_011511996.1:c.1069T>C	XP_011510298.1:p.Phe357Leu
XM_011511997.1:c.961T>C	XP_011510299.1:p.Phe321Leu
XM_011511994.3:c.1114T>C	XP_011510296.1:p.Phe372Leu
XM_011511996.2:c.1069T>C	XP_011510298.1:p.Phe357Leu
NM_003590.5:c.1261T>C MANE Select	NP_003581.1:p.Phe421Leu
NM_001257198.2:c.1279T>C	NP_001244127.1:p.Phe427Leu
NM_001257197.2:c.1063T>C	NP_001244126.1:p.Phe355Leu