Canonical Allele Identifier: CA3813351

Gene: CUL7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43040638C>T , CM000668.2:g.43040638C>T	GRCh38
NC_000006.11:g.43008376C>T , CM000668.1:g.43008376C>T	GRCh37
NC_000006.10:g.43116354C>T	NCBI36
NG_016205.1:g.18308G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014780.5:c.3915G>A MANE Select	NP_055595.2:p.Leu1305=
ENST00000265348.9:c.3915G>A MANE Select	ENSP00000265348.4:p.Leu1305=
NM_001168370.1:c.4167G>A	NP_001161842.1:p.Leu1389=
NM_001168370.2:c.4011G>A	NP_001161842.2:p.Leu1337=
NM_001374872.1:c.4011G>A	NP_001361801.1:p.Leu1337=
NM_001374873.1:c.3915G>A	NP_001361802.1:p.Leu1305=
NM_001374874.1:c.3912G>A	NP_001361803.1:p.Leu1304=
NM_014780.4:c.3915G>A	NP_055595.2:p.Leu1305=
ENST00000265348.7:c.3915G>A	ENSP00000265348.3:p.Leu1305=
ENST00000478630.2:n.1986G>A
ENST00000535468.1:c.4167G>A	ENSP00000438788.1:p.Leu1389=
ENST00000673725.1:c.1786G>A
ENST00000673753.1:n.4754G>A
ENST00000674100.1:c.4011G>A	ENSP00000501292.1:p.Leu1337=
ENST00000674112.1:c.2407G>A
ENST00000674112.2:c.3915G>A	ENSP00000501166.2:p.Leu1305=
ENST00000674134.1:c.4011G>A	ENSP00000501068.1:p.Leu1337=
ENST00000683320.1:n.276G>A
ENST00000685042.1:c.*571G>A	ENSP00000509871.1:n.*571G>A
ENST00000686442.1:n.4644G>A
ENST00000687225.1:c.*2212G>A	ENSP00000509364.1:n.*2212G>A
ENST00000688302.1:n.4198G>A
ENST00000689256.1:n.4492G>A
ENST00000690231.1:c.3915G>A	ENSP00000508461.1:p.Leu1305=
XM_005249503.1:c.4071G>A	XP_005249560.1:p.Leu1357=
XM_005249503.3:c.4071G>A	XP_005249560.1:p.Leu1357=
XM_006715285.1:c.4011G>A	XP_006715348.1:p.Leu1337=
XM_006715285.2:c.4011G>A	XP_006715348.1:p.Leu1337=
XM_011515019.1:c.4167G>A	XP_011513321.1:p.Leu1389=
XM_011515019.2:c.4167G>A	XP_011513321.1:p.Leu1389=
XM_011515020.1:c.4071G>A	XP_011513322.1:p.Leu1357=
XM_011515020.2:c.4071G>A	XP_011513322.1:p.Leu1357=
XM_011515021.1:c.1776G>A	XP_011513323.1:p.Leu592=
XM_017011533.1:c.4194G>A	XP_016867022.1:p.Leu1398=
XM_017011534.1:c.4194G>A	XP_016867023.1:p.Leu1398=
XM_017011535.1:c.4098G>A	XP_016867024.1:p.Leu1366=
XM_017011536.2:c.4038G>A	XP_016867025.1:p.Leu1346=
XM_017011537.2:c.4011G>A	XP_016867026.1:p.Leu1337=
XM_017011538.2:c.3942G>A	XP_016867027.1:p.Leu1314=
XM_017011539.2:c.3915G>A	XP_016867028.1:p.Leu1305=