Canonical Allele Identifier: CA1624354853

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042847_43042848delinsGC , CM000668.2:g.43042847_43042848delinsGC	GRCh38
NC_000006.11:g.43010585_43010586delinsGC , CM000668.1:g.43010585_43010586delinsGC	GRCh37
NC_000006.10:g.43118563_43118564delinsGC	NCBI36
NG_016205.1:g.16098_16099delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1670_1671delinsGC (CUL7)
ENST00000674112.2:c.3599_3600delinsGC (CUL7)	ENSP00000501166.2:p.Gly1200=
ENST00000685042.1:c.*255_*256delinsGC (CUL7)	ENSP00000509871.1:n.*255_*256delinsGC
ENST00000686442.1:n.4160_4161delinsGC (CUL7)
ENST00000687225.1:c.*1896_*1897delinsGC (CUL7)	ENSP00000509364.1:n.*1896_*1897delinsGC
ENST00000688302.1:n.3882_3883delinsGC (CUL7)
ENST00000689256.1:n.4176_4177delinsGC (CUL7)
ENST00000690231.1:c.3599_3600delinsGC (CUL7)	ENSP00000508461.1:p.Gly1200=
ENST00000265348.9:c.3599_3600delinsGC (CUL7) MANE Select	ENSP00000265348.4:p.Gly1200=
ENST00000673725.1:c.1470_1471delinsGC (CUL7)
ENST00000673753.1:n.4438_4439delinsGC (CUL7)
ENST00000674100.1:c.3695_3696delinsGC (CUL7)	ENSP00000501292.1:p.Gly1232=
ENST00000674112.1:c.2091_2092delinsGC (CUL7)
ENST00000674134.1:c.3695_3696delinsGC (CUL7)	ENSP00000501068.1:p.Gly1232=
ENST00000265348.7:c.3599_3600delinsGC (CUL7)	ENSP00000265348.3:p.Gly1200=
ENST00000467906.5:c.-1003-211_-1003-210delinsGC (KLC4)	ENSP00000418759.1:n.-1003-211_-1003-210delinsGC
ENST00000535468.1:c.3851_3852delinsGC (CUL7)	ENSP00000438788.1:p.Gly1284=
NM_001168370.1:c.3851_3852delinsGC (CUL7)	NP_001161842.1:p.Gly1284=
NM_014780.4:c.3599_3600delinsGC (CUL7)	NP_055595.2:p.Gly1200=
XM_005249503.1:c.3755_3756delinsGC (CUL7)	XP_005249560.1:p.Gly1252=
XM_006715285.1:c.3695_3696delinsGC (CUL7)	XP_006715348.1:p.Gly1232=
XM_011515019.1:c.3851_3852delinsGC (CUL7)	XP_011513321.1:p.Gly1284=
XM_011515020.1:c.3755_3756delinsGC (CUL7)	XP_011513322.1:p.Gly1252=
XM_011515021.1:c.1460_1461delinsGC (CUL7)	XP_011513323.1:p.Gly487=
XM_005249503.3:c.3755_3756delinsGC (CUL7)	XP_005249560.1:p.Gly1252=
XM_006715285.2:c.3695_3696delinsGC (CUL7)	XP_006715348.1:p.Gly1232=
XM_011515019.2:c.3851_3852delinsGC (CUL7)	XP_011513321.1:p.Gly1284=
XM_011515020.2:c.3755_3756delinsGC (CUL7)	XP_011513322.1:p.Gly1252=
XM_017011533.1:c.3878_3879delinsGC (CUL7)	XP_016867022.1:p.Gly1293=
XM_017011534.1:c.3878_3879delinsGC (CUL7)	XP_016867023.1:p.Gly1293=
XM_017011535.1:c.3782_3783delinsGC (CUL7)	XP_016867024.1:p.Gly1261=
XM_017011536.2:c.3722_3723delinsGC (CUL7)	XP_016867025.1:p.Gly1241=
XM_017011537.2:c.3695_3696delinsGC (CUL7)	XP_016867026.1:p.Gly1232=
XM_017011538.2:c.3626_3627delinsGC (CUL7)	XP_016867027.1:p.Gly1209=
XM_017011539.2:c.3599_3600delinsGC (CUL7)	XP_016867028.1:p.Gly1200=
NM_001168370.2:c.3695_3696delinsGC (CUL7)	NP_001161842.2:p.Gly1232=
NM_001374872.1:c.3695_3696delinsGC (CUL7)	NP_001361801.1:p.Gly1232=
NM_001374873.1:c.3599_3600delinsGC (CUL7)	NP_001361802.1:p.Gly1200=
NM_001374874.1:c.3596_3597delinsGC (CUL7)	NP_001361803.1:p.Gly1199=
NM_014780.5:c.3599_3600delinsGC (CUL7) MANE Select	NP_055595.2:p.Gly1200=