Canonical Allele Identifier: CA350827029

Gene: CUL3

Linked Data

• dbSNP Id: rs2106196663
• MyVariant Identifiers: chr2:g.225368400T>A (hg19) ; chr2:g.224503683T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503683T>A , CM000664.2:g.224503683T>A	GRCh38
NC_000002.11:g.225368400T>A , CM000664.1:g.225368400T>A	GRCh37
NC_000002.10:g.225076644T>A	NCBI36
NG_032169.1:g.86715A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1346A>T MANE Select	ENSP00000264414.4:p.Asp449Val
ENST00000264414.8:c.1346A>T	ENSP00000264414.4:p.Asp449Val
ENST00000344951.8:c.1148A>T	ENSP00000343601.4:p.Asp383Val
ENST00000409096.5:c.1274A>T	ENSP00000387200.1:p.Asp425Val
ENST00000409777.5:c.1274A>T	ENSP00000386525.1:p.Asp425Val
ENST00000481135.1:n.642A>T
ENST00000617432.4:c.70A>T	ENSP00000477851.1:p.Thr24Ser
NM_001257197.1:c.1148A>T	NP_001244126.1:p.Asp383Val
NM_001257198.1:c.1364A>T	NP_001244127.1:p.Asp455Val
NM_003590.4:c.1346A>T	NP_003581.1:p.Asp449Val
XM_006712800.2:c.1313A>T	XP_006712863.2:p.Asp438Val
XM_011511994.1:c.1199A>T	XP_011510296.1:p.Asp400Val
XM_011511995.1:c.1304A>T	XP_011510297.1:p.Asp435Val
XM_011511996.1:c.1154A>T	XP_011510298.1:p.Asp385Val
XM_011511997.1:c.1046A>T	XP_011510299.1:p.Asp349Val
XM_011511994.3:c.1199A>T	XP_011510296.1:p.Asp400Val
XM_011511996.2:c.1154A>T	XP_011510298.1:p.Asp385Val
NM_003590.5:c.1346A>T MANE Select	NP_003581.1:p.Asp449Val
NM_001257198.2:c.1364A>T	NP_001244127.1:p.Asp455Val
NM_001257197.2:c.1148A>T	NP_001244126.1:p.Asp383Val