Canonical Allele Identifier: CA450368901

Gene: CUL7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43038435C>T , CM000668.2:g.43038435C>T	GRCh38
NC_000006.11:g.43006173C>T , CM000668.1:g.43006173C>T	GRCh37
NC_000006.10:g.43114151C>T	NCBI36
NG_016205.1:g.20511G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014780.5:c.4605G>A MANE Select	NP_055595.2:p.Arg1535=
ENST00000265348.9:c.4605G>A MANE Select	ENSP00000265348.4:p.Arg1535=
NM_001168370.1:c.4857G>A	NP_001161842.1:p.Arg1619=
NM_001168370.2:c.4701G>A	NP_001161842.2:p.Arg1567=
NM_001374872.1:c.4701G>A	NP_001361801.1:p.Arg1567=
NM_001374873.1:c.4617G>A	NP_001361802.1:p.Arg1539=
NM_001374874.1:c.4602G>A	NP_001361803.1:p.Arg1534=
NM_014780.4:c.4605G>A	NP_055595.2:p.Arg1535=
ENST00000265348.7:c.4605G>A	ENSP00000265348.3:p.Arg1535=
ENST00000478630.2:n.2825G>A
ENST00000535468.1:c.4857G>A	ENSP00000438788.1:p.Arg1619=
ENST00000673725.1:c.2465G>A
ENST00000673753.1:n.5433G>A
ENST00000674100.1:c.4701G>A	ENSP00000501292.1:p.Arg1567=
ENST00000674112.1:c.3086G>A
ENST00000674112.2:c.4594G>A	ENSP00000501166.2:p.Val1532Ile
ENST00000674134.1:c.4701G>A	ENSP00000501068.1:p.Arg1567=
ENST00000683242.1:n.1152G>A
ENST00000685042.1:c.*1261G>A	ENSP00000509871.1:n.*1261G>A
ENST00000686442.1:n.5483G>A
ENST00000687225.1:c.*2891G>A	ENSP00000509364.1:n.*2891G>A
ENST00000688302.1:n.5026G>A
ENST00000689256.1:n.5182G>A
ENST00000690231.1:c.4605G>A	ENSP00000508461.1:p.Arg1535=
ENST00000692002.1:c.630G>A	ENSP00000508567.1:p.Arg210=
XM_005249503.1:c.4761G>A	XP_005249560.1:p.Arg1587=
XM_005249503.3:c.4761G>A	XP_005249560.1:p.Arg1587=
XM_006715285.1:c.4713G>A	XP_006715348.1:p.Arg1571=
XM_006715285.2:c.4713G>A	XP_006715348.1:p.Arg1571=
XM_011515019.1:c.4869G>A	XP_011513321.1:p.Arg1623=
XM_011515019.2:c.4869G>A	XP_011513321.1:p.Arg1623=
XM_011515020.1:c.4773G>A	XP_011513322.1:p.Arg1591=
XM_011515020.2:c.4773G>A	XP_011513322.1:p.Arg1591=
XM_011515021.1:c.2478G>A	XP_011513323.1:p.Arg826=
XM_017011533.1:c.4896G>A	XP_016867022.1:p.Arg1632=
XM_017011534.1:c.4884G>A	XP_016867023.1:p.Arg1628=
XM_017011535.1:c.4800G>A	XP_016867024.1:p.Arg1600=
XM_017011536.2:c.4740G>A	XP_016867025.1:p.Arg1580=
XM_017011537.2:c.4701G>A	XP_016867026.1:p.Arg1567=
XM_017011538.2:c.4644G>A	XP_016867027.1:p.Arg1548=
XM_017011539.2:c.4617G>A	XP_016867028.1:p.Arg1539=