Canonical Allele Identifier: CA1624354926

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043044_43043046delinsCCT , CM000668.2:g.43043044_43043046delinsCCT	GRCh38
NC_000006.11:g.43010782_43010784delinsCCT , CM000668.1:g.43010782_43010784delinsCCT	GRCh37
NC_000006.10:g.43118760_43118762delinsCCT	NCBI36
NG_016205.1:g.15900_15902delinsAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000478630.2:n.1533+28_1533+30delinsAGG (CUL7)
ENST00000674112.2:c.3462+28_3462+30delinsAGG (CUL7)	ENSP00000501166.2:n.3462+28_3462+30delins...
ENST00000685042.1:c.*118+28_*118+30delinsAGG (CUL7)	ENSP00000509871.1:n.*118+28_*118+30delins...
ENST00000686442.1:n.4023+28_4023+30delinsAGG (CUL7)
ENST00000687225.1:c.*1759+28_*1759+30delinsAGG (CUL7)	ENSP00000509364.1:n.*1759+28_*1759+30deli...
ENST00000688302.1:n.3745+28_3745+30delinsAGG (CUL7)
ENST00000689256.1:n.4039+28_4039+30delinsAGG (CUL7)
ENST00000690231.1:c.3462+28_3462+30delinsAGG (CUL7)	ENSP00000508461.1:n.3462+28_3462+30delins...
ENST00000265348.9:c.3462+28_3462+30delinsAGG (CUL7) MANE Select	ENSP00000265348.4:n.3462+28_3462+30delins...
ENST00000673725.1:c.1411+28_1411+30delinsAGG (CUL7)
ENST00000673753.1:n.4301+28_4301+30delinsAGG (CUL7)
ENST00000674100.1:c.3558+28_3558+30delinsAGG (CUL7)	ENSP00000501292.1:n.3558+28_3558+30delins...
ENST00000674112.1:c.1954+28_1954+30delinsAGG (CUL7)
ENST00000674134.1:c.3558+28_3558+30delinsAGG (CUL7)	ENSP00000501068.1:n.3558+28_3558+30delins...
ENST00000265348.7:c.3462+28_3462+30delinsAGG (CUL7)	ENSP00000265348.3:n.3462+28_3462+30delins...
ENST00000467906.5:c.-1003-14_-1003-12delinsCCT (KLC4)	ENSP00000418759.1:n.-1003-14_-1003-12deli...
ENST00000535468.1:c.3714+28_3714+30delinsAGG (CUL7)	ENSP00000438788.1:n.3714+28_3714+30delins...
NM_001168370.1:c.3714+28_3714+30delinsAGG (CUL7)	NP_001161842.1:n.3714+28_3714+30delinsAGG...
NM_014780.4:c.3462+28_3462+30delinsAGG (CUL7)	NP_055595.2:n.3462+28_3462+30delinsAGG
XM_005249503.1:c.3618+28_3618+30delinsAGG (CUL7)	XP_005249560.1:n.3618+28_3618+30delinsAGG...
XM_006715285.1:c.3558+28_3558+30delinsAGG (CUL7)	XP_006715348.1:n.3558+28_3558+30delinsAGG...
XM_011515019.1:c.3714+28_3714+30delinsAGG (CUL7)	XP_011513321.1:n.3714+28_3714+30delinsAGG...
XM_011515020.1:c.3618+28_3618+30delinsAGG (CUL7)	XP_011513322.1:n.3618+28_3618+30delinsAGG...
XM_011515021.1:c.1323+28_1323+30delinsAGG (CUL7)	XP_011513323.1:n.1323+28_1323+30delinsAGG...
XM_005249503.3:c.3618+28_3618+30delinsAGG (CUL7)	XP_005249560.1:n.3618+28_3618+30delinsAGG...
XM_006715285.2:c.3558+28_3558+30delinsAGG (CUL7)	XP_006715348.1:n.3558+28_3558+30delinsAGG...
XM_011515019.2:c.3714+28_3714+30delinsAGG (CUL7)	XP_011513321.1:n.3714+28_3714+30delinsAGG...
XM_011515020.2:c.3618+28_3618+30delinsAGG (CUL7)	XP_011513322.1:n.3618+28_3618+30delinsAGG...
XM_017011533.1:c.3741+28_3741+30delinsAGG (CUL7)	XP_016867022.1:n.3741+28_3741+30delinsAGG...
XM_017011534.1:c.3741+28_3741+30delinsAGG (CUL7)	XP_016867023.1:n.3741+28_3741+30delinsAGG...
XM_017011535.1:c.3645+28_3645+30delinsAGG (CUL7)	XP_016867024.1:n.3645+28_3645+30delinsAGG...
XM_017011536.2:c.3585+28_3585+30delinsAGG (CUL7)	XP_016867025.1:n.3585+28_3585+30delinsAGG...
XM_017011537.2:c.3558+28_3558+30delinsAGG (CUL7)	XP_016867026.1:n.3558+28_3558+30delinsAGG...
XM_017011538.2:c.3489+28_3489+30delinsAGG (CUL7)	XP_016867027.1:n.3489+28_3489+30delinsAGG...
XM_017011539.2:c.3462+28_3462+30delinsAGG (CUL7)	XP_016867028.1:n.3462+28_3462+30delinsAGG...
NM_001168370.2:c.3558+28_3558+30delinsAGG (CUL7)	NP_001161842.2:n.3558+28_3558+30delinsAGG...
NM_001374872.1:c.3558+28_3558+30delinsAGG (CUL7)	NP_001361801.1:n.3558+28_3558+30delinsAGG...
NM_001374873.1:c.3462+28_3462+30delinsAGG (CUL7)	NP_001361802.1:n.3462+28_3462+30delinsAGG...
NM_001374874.1:c.3459+28_3459+30delinsAGG (CUL7)	NP_001361803.1:n.3459+28_3459+30delinsAGG...
NM_014780.5:c.3462+28_3462+30delinsAGG (CUL7) MANE Select	NP_055595.2:n.3462+28_3462+30delinsAGG