Canonical Allele Identifier: CA350827553

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368482T>C (hg19) ; chr2:g.224503765T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503765T>C , CM000664.2:g.224503765T>C	GRCh38
NC_000002.11:g.225368482T>C , CM000664.1:g.225368482T>C	GRCh37
NC_000002.10:g.225076726T>C	NCBI36
NG_032169.1:g.86633A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1264A>G MANE Select	ENSP00000264414.4:p.Met422Val
ENST00000264414.8:c.1264A>G	ENSP00000264414.4:p.Met422Val
ENST00000344951.8:c.1066A>G	ENSP00000343601.4:p.Met356Val
ENST00000409096.5:c.1192A>G	ENSP00000387200.1:p.Met398Val
ENST00000409777.5:c.1192A>G	ENSP00000386525.1:p.Met398Val
ENST00000481135.1:n.560A>G
ENST00000617432.4:c.-13A>G	ENSP00000477851.1:n.-13A>G
NM_001257197.1:c.1066A>G	NP_001244126.1:p.Met356Val
NM_001257198.1:c.1282A>G	NP_001244127.1:p.Met428Val
NM_003590.4:c.1264A>G	NP_003581.1:p.Met422Val
XM_006712800.2:c.1231A>G	XP_006712863.2:p.Met411Val
XM_011511994.1:c.1117A>G	XP_011510296.1:p.Met373Val
XM_011511995.1:c.1222A>G	XP_011510297.1:p.Met408Val
XM_011511996.1:c.1072A>G	XP_011510298.1:p.Met358Val
XM_011511997.1:c.964A>G	XP_011510299.1:p.Met322Val
XM_011511994.3:c.1117A>G	XP_011510296.1:p.Met373Val
XM_011511996.2:c.1072A>G	XP_011510298.1:p.Met358Val
NM_003590.5:c.1264A>G MANE Select	NP_003581.1:p.Met422Val
NM_001257198.2:c.1282A>G	NP_001244127.1:p.Met428Val
NM_001257197.2:c.1066A>G	NP_001244126.1:p.Met356Val