Canonical Allele Identifier: CA350827540

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197232
• MyVariant Identifiers: chr2:g.225368478T>A (hg19) ; chr2:g.224503761T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503761T>A , CM000664.2:g.224503761T>A	GRCh38
NC_000002.11:g.225368478T>A , CM000664.1:g.225368478T>A	GRCh37
NC_000002.10:g.225076722T>A	NCBI36
NG_032169.1:g.86637A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1268A>T MANE Select	ENSP00000264414.4:p.Gln423Leu
ENST00000264414.8:c.1268A>T	ENSP00000264414.4:p.Gln423Leu
ENST00000344951.8:c.1070A>T	ENSP00000343601.4:p.Gln357Leu
ENST00000409096.5:c.1196A>T	ENSP00000387200.1:p.Gln399Leu
ENST00000409777.5:c.1196A>T	ENSP00000386525.1:p.Gln399Leu
ENST00000481135.1:n.564A>T
ENST00000617432.4:c.-9A>T	ENSP00000477851.1:n.-9A>T
NM_001257197.1:c.1070A>T	NP_001244126.1:p.Gln357Leu
NM_001257198.1:c.1286A>T	NP_001244127.1:p.Gln429Leu
NM_003590.4:c.1268A>T	NP_003581.1:p.Gln423Leu
XM_006712800.2:c.1235A>T	XP_006712863.2:p.Gln412Leu
XM_011511994.1:c.1121A>T	XP_011510296.1:p.Gln374Leu
XM_011511995.1:c.1226A>T	XP_011510297.1:p.Gln409Leu
XM_011511996.1:c.1076A>T	XP_011510298.1:p.Gln359Leu
XM_011511997.1:c.968A>T	XP_011510299.1:p.Gln323Leu
XM_011511994.3:c.1121A>T	XP_011510296.1:p.Gln374Leu
XM_011511996.2:c.1076A>T	XP_011510298.1:p.Gln359Leu
NM_003590.5:c.1268A>T MANE Select	NP_003581.1:p.Gln423Leu
NM_001257198.2:c.1286A>T	NP_001244127.1:p.Gln429Leu
NM_001257197.2:c.1070A>T	NP_001244126.1:p.Gln357Leu