Canonical Allele Identifier: CA66553945

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224535798T>A , CM000664.2:g.224535798T>A	GRCh38
NC_000002.11:g.225400515T>A , CM000664.1:g.225400515T>A	GRCh37
NC_000002.10:g.225108759T>A	NCBI36
NG_032169.1:g.54600A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003590.5:c.265-157A>T MANE Select	NP_003581.1:n.265-157A>T
ENST00000264414.9:c.265-157A>T MANE Select	ENSP00000264414.4:n.265-157A>T
NM_001257197.1:c.67-157A>T	NP_001244126.1:n.67-157A>T
NM_001257197.2:c.67-157A>T	NP_001244126.1:n.67-157A>T
NM_001257198.1:c.283-157A>T	NP_001244127.1:n.283-157A>T
NM_001257198.2:c.283-157A>T	NP_001244127.1:n.283-157A>T
NM_003590.4:c.265-157A>T	NP_003581.1:n.265-157A>T
ENST00000264414.8:c.265-157A>T	ENSP00000264414.4:n.265-157A>T
ENST00000344951.8:c.67-157A>T	ENSP00000343601.4:n.67-157A>T
ENST00000409096.5:c.193-157A>T	ENSP00000387200.1:n.193-157A>T
ENST00000409777.5:c.193-157A>T	ENSP00000386525.1:n.193-157A>T
ENST00000432260.2:c.289-157A>T	ENSP00000484410.1:n.289-157A>T
ENST00000436172.1:c.326-157A>T
ENST00000546102.1:n.523-157A>T
XM_006712800.2:c.232-157A>T	XP_006712863.2:n.232-157A>T
XM_011511994.1:c.232-21026A>T	XP_011510296.1:n.232-21026A>T
XM_011511994.3:c.232-21026A>T	XP_011510296.1:n.232-21026A>T
XM_011511995.1:c.223-157A>T	XP_011510297.1:n.223-157A>T
XM_011511996.1:c.73-157A>T	XP_011510298.1:n.73-157A>T
XM_011511996.2:c.73-157A>T	XP_011510298.1:n.73-157A>T