Canonical Allele Identifier: CA350827520

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197197
• MyVariant Identifiers: chr2:g.225368470C>T (hg19) ; chr2:g.224503753C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503753C>T , CM000664.2:g.224503753C>T	GRCh38
NC_000002.11:g.225368470C>T , CM000664.1:g.225368470C>T	GRCh37
NC_000002.10:g.225076714C>T	NCBI36
NG_032169.1:g.86645G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1276G>A MANE Select	ENSP00000264414.4:p.Asp426Asn
ENST00000264414.8:c.1276G>A	ENSP00000264414.4:p.Asp426Asn
ENST00000344951.8:c.1078G>A	ENSP00000343601.4:p.Asp360Asn
ENST00000409096.5:c.1204G>A	ENSP00000387200.1:p.Asp402Asn
ENST00000409777.5:c.1204G>A	ENSP00000386525.1:p.Asp402Asn
ENST00000481135.1:n.572G>A
ENST00000617432.4:c.-1G>A	ENSP00000477851.1:n.-1G>A
NM_001257197.1:c.1078G>A	NP_001244126.1:p.Asp360Asn
NM_001257198.1:c.1294G>A	NP_001244127.1:p.Asp432Asn
NM_003590.4:c.1276G>A	NP_003581.1:p.Asp426Asn
XM_006712800.2:c.1243G>A	XP_006712863.2:p.Asp415Asn
XM_011511994.1:c.1129G>A	XP_011510296.1:p.Asp377Asn
XM_011511995.1:c.1234G>A	XP_011510297.1:p.Asp412Asn
XM_011511996.1:c.1084G>A	XP_011510298.1:p.Asp362Asn
XM_011511997.1:c.976G>A	XP_011510299.1:p.Asp326Asn
XM_011511994.3:c.1129G>A	XP_011510296.1:p.Asp377Asn
XM_011511996.2:c.1084G>A	XP_011510298.1:p.Asp362Asn
NM_003590.5:c.1276G>A MANE Select	NP_003581.1:p.Asp426Asn
NM_001257198.2:c.1294G>A	NP_001244127.1:p.Asp432Asn
NM_001257197.2:c.1078G>A	NP_001244126.1:p.Asp360Asn