Canonical Allele Identifier: CA350827026

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368399G>T (hg19) ; chr2:g.224503682G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503682G>T , CM000664.2:g.224503682G>T	GRCh38
NC_000002.11:g.225368399G>T , CM000664.1:g.225368399G>T	GRCh37
NC_000002.10:g.225076643G>T	NCBI36
NG_032169.1:g.86716C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1347C>A MANE Select	ENSP00000264414.4:p.Asp449Glu
ENST00000264414.8:c.1347C>A	ENSP00000264414.4:p.Asp449Glu
ENST00000344951.8:c.1149C>A	ENSP00000343601.4:p.Asp383Glu
ENST00000409096.5:c.1275C>A	ENSP00000387200.1:p.Asp425Glu
ENST00000409777.5:c.1275C>A	ENSP00000386525.1:p.Asp425Glu
ENST00000481135.1:n.643C>A
ENST00000617432.4:c.71C>A	ENSP00000477851.1:p.Thr24Asn
NM_001257197.1:c.1149C>A	NP_001244126.1:p.Asp383Glu
NM_001257198.1:c.1365C>A	NP_001244127.1:p.Asp455Glu
NM_003590.4:c.1347C>A	NP_003581.1:p.Asp449Glu
XM_006712800.2:c.1314C>A	XP_006712863.2:p.Asp438Glu
XM_011511994.1:c.1200C>A	XP_011510296.1:p.Asp400Glu
XM_011511995.1:c.1305C>A	XP_011510297.1:p.Asp435Glu
XM_011511996.1:c.1155C>A	XP_011510298.1:p.Asp385Glu
XM_011511997.1:c.1047C>A	XP_011510299.1:p.Asp349Glu
XM_011511994.3:c.1200C>A	XP_011510296.1:p.Asp400Glu
XM_011511996.2:c.1155C>A	XP_011510298.1:p.Asp385Glu
NM_003590.5:c.1347C>A MANE Select	NP_003581.1:p.Asp449Glu
NM_001257198.2:c.1365C>A	NP_001244127.1:p.Asp455Glu
NM_001257197.2:c.1149C>A	NP_001244126.1:p.Asp383Glu