Canonical Allele Identifier: CA350827610

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368496A>T (hg19) ; chr2:g.224503779A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503779A>T , CM000664.2:g.224503779A>T	GRCh38
NC_000002.11:g.225368496A>T , CM000664.1:g.225368496A>T	GRCh37
NC_000002.10:g.225076740A>T	NCBI36
NG_032169.1:g.86619T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1250T>A MANE Select	ENSP00000264414.4:p.Val417Asp
ENST00000264414.8:c.1250T>A	ENSP00000264414.4:p.Val417Asp
ENST00000344951.8:c.1052T>A	ENSP00000343601.4:p.Val351Asp
ENST00000409096.5:c.1178T>A	ENSP00000387200.1:p.Val393Asp
ENST00000409777.5:c.1178T>A	ENSP00000386525.1:p.Val393Asp
ENST00000481135.1:n.546T>A
ENST00000617432.4:c.-27T>A	ENSP00000477851.1:n.-27T>A
NM_001257197.1:c.1052T>A	NP_001244126.1:p.Val351Asp
NM_001257198.1:c.1268T>A	NP_001244127.1:p.Val423Asp
NM_003590.4:c.1250T>A	NP_003581.1:p.Val417Asp
XM_006712800.2:c.1217T>A	XP_006712863.2:p.Val406Asp
XM_011511994.1:c.1103T>A	XP_011510296.1:p.Val368Asp
XM_011511995.1:c.1208T>A	XP_011510297.1:p.Val403Asp
XM_011511996.1:c.1058T>A	XP_011510298.1:p.Val353Asp
XM_011511997.1:c.950T>A	XP_011510299.1:p.Val317Asp
XM_011511994.3:c.1103T>A	XP_011510296.1:p.Val368Asp
XM_011511996.2:c.1058T>A	XP_011510298.1:p.Val353Asp
NM_003590.5:c.1250T>A MANE Select	NP_003581.1:p.Val417Asp
NM_001257198.2:c.1268T>A	NP_001244127.1:p.Val423Asp
NM_001257197.2:c.1052T>A	NP_001244126.1:p.Val351Asp