Canonical Allele Identifier: CA3813238

Gene: CUL7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43038964G>A , CM000668.2:g.43038964G>A	GRCh38
NC_000006.11:g.43006702G>A , CM000668.1:g.43006702G>A	GRCh37
NC_000006.10:g.43114680G>A	NCBI36
NG_016205.1:g.19982C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014780.5:c.4318C>T MANE Select	NP_055595.2:p.Arg1440Ter
ENST00000265348.9:c.4318C>T MANE Select	ENSP00000265348.4:p.Arg1440Ter
NM_001168370.1:c.4570C>T	NP_001161842.1:p.Arg1524Ter
NM_001168370.2:c.4414C>T	NP_001161842.2:p.Arg1472Ter
NM_001374872.1:c.4414C>T	NP_001361801.1:p.Arg1472Ter
NM_001374873.1:c.4318C>T	NP_001361802.1:p.Arg1440Ter
NM_001374874.1:c.4315C>T	NP_001361803.1:p.Arg1439Ter
NM_014780.4:c.4318C>T	NP_055595.2:p.Arg1440Ter
ENST00000265348.7:c.4318C>T	ENSP00000265348.3:p.Arg1440Ter
ENST00000478630.2:n.2389C>T
ENST00000535468.1:c.4570C>T	ENSP00000438788.1:p.Arg1524Ter
ENST00000673725.1:c.2189C>T
ENST00000673753.1:n.5157C>T
ENST00000674100.1:c.4414C>T	ENSP00000501292.1:p.Arg1472Ter
ENST00000674112.1:c.2810C>T
ENST00000674112.2:c.4318C>T	ENSP00000501166.2:p.Arg1440Ter
ENST00000674134.1:c.4414C>T	ENSP00000501068.1:p.Arg1472Ter
ENST00000683242.1:n.716C>T
ENST00000685042.1:c.*974C>T	ENSP00000509871.1:n.*974C>T
ENST00000686442.1:n.5047C>T
ENST00000687225.1:c.*2615C>T	ENSP00000509364.1:n.*2615C>T
ENST00000688302.1:n.4601C>T
ENST00000689256.1:n.4895C>T
ENST00000690231.1:c.4318C>T	ENSP00000508461.1:p.Arg1440Ter
ENST00000692002.1:c.331C>T	ENSP00000508567.1:p.Arg111Ter
XM_005249503.1:c.4474C>T	XP_005249560.1:p.Arg1492Ter
XM_005249503.3:c.4474C>T	XP_005249560.1:p.Arg1492Ter
XM_006715285.1:c.4414C>T	XP_006715348.1:p.Arg1472Ter
XM_006715285.2:c.4414C>T	XP_006715348.1:p.Arg1472Ter
XM_011515019.1:c.4570C>T	XP_011513321.1:p.Arg1524Ter
XM_011515019.2:c.4570C>T	XP_011513321.1:p.Arg1524Ter
XM_011515020.1:c.4474C>T	XP_011513322.1:p.Arg1492Ter
XM_011515020.2:c.4474C>T	XP_011513322.1:p.Arg1492Ter
XM_011515021.1:c.2179C>T	XP_011513323.1:p.Arg727Ter
XM_017011533.1:c.4597C>T	XP_016867022.1:p.Arg1533Ter
XM_017011534.1:c.4597C>T	XP_016867023.1:p.Arg1533Ter
XM_017011535.1:c.4501C>T	XP_016867024.1:p.Arg1501Ter
XM_017011536.2:c.4441C>T	XP_016867025.1:p.Arg1481Ter
XM_017011537.2:c.4414C>T	XP_016867026.1:p.Arg1472Ter
XM_017011538.2:c.4345C>T	XP_016867027.1:p.Arg1449Ter
XM_017011539.2:c.4318C>T	XP_016867028.1:p.Arg1440Ter