Canonical Allele Identifier: CA1624354863

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042868G= , CM000668.2:g.43042868G=	GRCh38
NC_000006.11:g.43010606G= , CM000668.1:g.43010606G=	GRCh37
NC_000006.10:g.43118584G=	NCBI36
NG_016205.1:g.16078C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000478630.2:n.1650C= (CUL7)
ENST00000674112.2:c.3579C= (CUL7)	ENSP00000501166.2:p.Phe1193=
ENST00000685042.1:c.*235C= (CUL7)	ENSP00000509871.1:n.*235C=
ENST00000686442.1:n.4140C= (CUL7)
ENST00000687225.1:c.*1876C= (CUL7)	ENSP00000509364.1:n.*1876C=
ENST00000688302.1:n.3862C= (CUL7)
ENST00000689256.1:n.4156C= (CUL7)
ENST00000690231.1:c.3579C= (CUL7)	ENSP00000508461.1:p.Phe1193=
ENST00000265348.9:c.3579C= (CUL7) MANE Select	ENSP00000265348.4:p.Phe1193=
ENST00000673725.1:c.1450C= (CUL7)
ENST00000673753.1:n.4418C= (CUL7)
ENST00000674100.1:c.3675C= (CUL7)	ENSP00000501292.1:p.Phe1225=
ENST00000674112.1:c.2071C= (CUL7)
ENST00000674134.1:c.3675C= (CUL7)	ENSP00000501068.1:p.Phe1225=
ENST00000265348.7:c.3579C= (CUL7)	ENSP00000265348.3:p.Phe1193=
ENST00000467906.5:c.-1003-190G= (KLC4)	ENSP00000418759.1:n.-1003-190G=
ENST00000535468.1:c.3831C= (CUL7)	ENSP00000438788.1:p.Phe1277=
NM_001168370.1:c.3831C= (CUL7)	NP_001161842.1:p.Phe1277=
NM_014780.4:c.3579C= (CUL7)	NP_055595.2:p.Phe1193=
XM_005249503.1:c.3735C= (CUL7)	XP_005249560.1:p.Phe1245=
XM_006715285.1:c.3675C= (CUL7)	XP_006715348.1:p.Phe1225=
XM_011515019.1:c.3831C= (CUL7)	XP_011513321.1:p.Phe1277=
XM_011515020.1:c.3735C= (CUL7)	XP_011513322.1:p.Phe1245=
XM_011515021.1:c.1440C= (CUL7)	XP_011513323.1:p.Phe480=
XM_005249503.3:c.3735C= (CUL7)	XP_005249560.1:p.Phe1245=
XM_006715285.2:c.3675C= (CUL7)	XP_006715348.1:p.Phe1225=
XM_011515019.2:c.3831C= (CUL7)	XP_011513321.1:p.Phe1277=
XM_011515020.2:c.3735C= (CUL7)	XP_011513322.1:p.Phe1245=
XM_017011533.1:c.3858C= (CUL7)	XP_016867022.1:p.Phe1286=
XM_017011534.1:c.3858C= (CUL7)	XP_016867023.1:p.Phe1286=
XM_017011535.1:c.3762C= (CUL7)	XP_016867024.1:p.Phe1254=
XM_017011536.2:c.3702C= (CUL7)	XP_016867025.1:p.Phe1234=
XM_017011537.2:c.3675C= (CUL7)	XP_016867026.1:p.Phe1225=
XM_017011538.2:c.3606C= (CUL7)	XP_016867027.1:p.Phe1202=
XM_017011539.2:c.3579C= (CUL7)	XP_016867028.1:p.Phe1193=
NM_001168370.2:c.3675C= (CUL7)	NP_001161842.2:p.Phe1225=
NM_001374872.1:c.3675C= (CUL7)	NP_001361801.1:p.Phe1225=
NM_001374873.1:c.3579C= (CUL7)	NP_001361802.1:p.Phe1193=
NM_001374874.1:c.3576C= (CUL7)	NP_001361803.1:p.Phe1192=
NM_014780.5:c.3579C= (CUL7) MANE Select	NP_055595.2:p.Phe1193=