Canonical Allele Identifier: CA1624354979

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043156C= , CM000668.2:g.43043156C=	GRCh38
NC_000006.11:g.43010894C= , CM000668.1:g.43010894C=	GRCh37
NC_000006.10:g.43118872C=	NCBI36
NG_016205.1:g.15790G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1451G= (CUL7)
ENST00000674112.2:c.3380G= (CUL7)	ENSP00000501166.2:p.Trp1127=
ENST00000685042.1:c.*36G= (CUL7)	ENSP00000509871.1:n.*36G=
ENST00000686442.1:n.3941G= (CUL7)
ENST00000687225.1:c.*1677G= (CUL7)	ENSP00000509364.1:n.*1677G=
ENST00000688302.1:n.3663G= (CUL7)
ENST00000689256.1:n.3957G= (CUL7)
ENST00000690231.1:c.3380G= (CUL7)	ENSP00000508461.1:p.Trp1127=
ENST00000265348.9:c.3380G= (CUL7) MANE Select	ENSP00000265348.4:p.Trp1127=
ENST00000673725.1:c.1329G= (CUL7)
ENST00000673753.1:n.4219G= (CUL7)
ENST00000674100.1:c.3476G= (CUL7)	ENSP00000501292.1:p.Trp1159=
ENST00000674112.1:c.1872G= (CUL7)
ENST00000674134.1:c.3476G= (CUL7)	ENSP00000501068.1:p.Trp1159=
ENST00000265348.7:c.3380G= (CUL7)	ENSP00000265348.3:p.Trp1127=
ENST00000467906.5:c.-905C= (KLC4)	ENSP00000418759.1:n.-905C=
ENST00000535468.1:c.3632G= (CUL7)	ENSP00000438788.1:p.Trp1211=
NM_001168370.1:c.3632G= (CUL7)	NP_001161842.1:p.Trp1211=
NM_014780.4:c.3380G= (CUL7)	NP_055595.2:p.Trp1127=
XM_005249503.1:c.3536G= (CUL7)	XP_005249560.1:p.Trp1179=
XM_006715285.1:c.3476G= (CUL7)	XP_006715348.1:p.Trp1159=
XM_011515019.1:c.3632G= (CUL7)	XP_011513321.1:p.Trp1211=
XM_011515020.1:c.3536G= (CUL7)	XP_011513322.1:p.Trp1179=
XM_011515021.1:c.1241G= (CUL7)	XP_011513323.1:p.Trp414=
XM_005249503.3:c.3536G= (CUL7)	XP_005249560.1:p.Trp1179=
XM_006715285.2:c.3476G= (CUL7)	XP_006715348.1:p.Trp1159=
XM_011515019.2:c.3632G= (CUL7)	XP_011513321.1:p.Trp1211=
XM_011515020.2:c.3536G= (CUL7)	XP_011513322.1:p.Trp1179=
XM_017011533.1:c.3659G= (CUL7)	XP_016867022.1:p.Trp1220=
XM_017011534.1:c.3659G= (CUL7)	XP_016867023.1:p.Trp1220=
XM_017011535.1:c.3563G= (CUL7)	XP_016867024.1:p.Trp1188=
XM_017011536.2:c.3503G= (CUL7)	XP_016867025.1:p.Trp1168=
XM_017011537.2:c.3476G= (CUL7)	XP_016867026.1:p.Trp1159=
XM_017011538.2:c.3407G= (CUL7)	XP_016867027.1:p.Trp1136=
XM_017011539.2:c.3380G= (CUL7)	XP_016867028.1:p.Trp1127=
NM_001168370.2:c.3476G= (CUL7)	NP_001161842.2:p.Trp1159=
NM_001374872.1:c.3476G= (CUL7)	NP_001361801.1:p.Trp1159=
NM_001374873.1:c.3380G= (CUL7)	NP_001361802.1:p.Trp1127=
NM_001374874.1:c.3377G= (CUL7)	NP_001361803.1:p.Trp1126=
NM_014780.5:c.3380G= (CUL7) MANE Select	NP_055595.2:p.Trp1127=