Canonical Allele Identifier: CA350826882

Gene: CUL3

Linked Data

• dbSNP Id: rs2106196435
• MyVariant Identifiers: chr2:g.225368372T>A (hg19) ; chr2:g.224503655T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503655T>A , CM000664.2:g.224503655T>A	GRCh38
NC_000002.11:g.225368372T>A , CM000664.1:g.225368372T>A	GRCh37
NC_000002.10:g.225076616T>A	NCBI36
NG_032169.1:g.86743A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1374A>T MANE Select	ENSP00000264414.4:p.Leu458Phe
ENST00000264414.8:c.1374A>T	ENSP00000264414.4:p.Leu458Phe
ENST00000344951.8:c.1176A>T	ENSP00000343601.4:p.Leu392Phe
ENST00000409096.5:c.1302A>T	ENSP00000387200.1:p.Leu434Phe
ENST00000409777.5:c.1302A>T	ENSP00000386525.1:p.Leu434Phe
ENST00000481135.1:n.670A>T
ENST00000617432.4:c.96A>T	ENSP00000477851.1:p.Leu32Phe
NM_001257197.1:c.1176A>T	NP_001244126.1:p.Leu392Phe
NM_001257198.1:c.1392A>T	NP_001244127.1:p.Leu464Phe
NM_003590.4:c.1374A>T	NP_003581.1:p.Leu458Phe
XM_006712800.2:c.1341A>T	XP_006712863.2:p.Leu447Phe
XM_011511994.1:c.1227A>T	XP_011510296.1:p.Leu409Phe
XM_011511995.1:c.1332A>T	XP_011510297.1:p.Leu444Phe
XM_011511996.1:c.1182A>T	XP_011510298.1:p.Leu394Phe
XM_011511997.1:c.1074A>T	XP_011510299.1:p.Leu358Phe
XM_011511994.3:c.1227A>T	XP_011510296.1:p.Leu409Phe
XM_011511996.2:c.1182A>T	XP_011510298.1:p.Leu394Phe
NM_003590.5:c.1374A>T MANE Select	NP_003581.1:p.Leu458Phe
NM_001257198.2:c.1392A>T	NP_001244127.1:p.Leu464Phe
NM_001257197.2:c.1176A>T	NP_001244126.1:p.Leu392Phe