Canonical Allele Identifier: CA1624358344

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43050699_43050700delinsTC , CM000668.2:g.43050699_43050700delinsTC	GRCh38
NC_000006.11:g.43018437_43018438delinsTC , CM000668.1:g.43018437_43018438delinsTC	GRCh37
NC_000006.10:g.43126415_43126416delinsTC	NCBI36
NG_016205.1:g.8246_8247delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.1233+268_1233+269delinsGA (CUL7)	ENSP00000501166.2:n.1233+268_1233+269delinsGA
ENST00000683160.1:n.1615+268_1615+269delinsGA (CUL7)
ENST00000683493.1:n.1274+268_1274+269delinsGA (CUL7)
ENST00000685042.1:c.1233+268_1233+269delinsGA (CUL7)	ENSP00000509871.1:n.1233+268_1233+269delinsGA
ENST00000686442.1:n.1516+268_1516+269delinsGA (CUL7)
ENST00000687225.1:c.1329+268_1329+269delinsGA (CUL7)	ENSP00000509364.1:n.1329+268_1329+269delinsGA
ENST00000688302.1:n.1516+268_1516+269delinsGA (CUL7)
ENST00000688707.1:c.1329+268_1329+269delinsGA (CUL7)	ENSP00000510608.1:n.1329+268_1329+269delinsGA
ENST00000689256.1:n.1532+268_1532+269delinsGA (CUL7)
ENST00000690231.1:c.1233+268_1233+269delinsGA (CUL7)	ENSP00000508461.1:n.1233+268_1233+269delinsGA
ENST00000265348.9:c.1233+268_1233+269delinsGA (CUL7) MANE Select	ENSP00000265348.4:n.1233+268_1233+269delinsGA
ENST00000673753.1:n.1567+268_1567+269delinsGA (CUL7)
ENST00000674100.1:c.1329+268_1329+269delinsGA (CUL7)	ENSP00000501292.1:n.1329+268_1329+269delinsGA
ENST00000674134.1:c.1329+268_1329+269delinsGA (CUL7)	ENSP00000501068.1:n.1329+268_1329+269delinsGA
ENST00000265348.7:c.1233+268_1233+269delinsGA (CUL7)	ENSP00000265348.3:n.1233+268_1233+269delinsGA
ENST00000467906.5:c.-553+7191_-553+7192delinsTC (KLC4)	ENSP00000418759.1:n.-553+7191_-553+7192delinsTC
ENST00000535468.1:c.1485+268_1485+269delinsGA (CUL7)	ENSP00000438788.1:n.1485+268_1485+269delinsGA
NM_001168370.1:c.1485+268_1485+269delinsGA (CUL7)	NP_001161842.1:n.1485+268_1485+269delinsGA
NM_014780.4:c.1233+268_1233+269delinsGA (CUL7)	NP_055595.2:n.1233+268_1233+269delinsGA
XM_005249503.1:c.1389+268_1389+269delinsGA (CUL7)	XP_005249560.1:n.1389+268_1389+269delinsGA
XM_006715285.1:c.1329+268_1329+269delinsGA (CUL7)	XP_006715348.1:n.1329+268_1329+269delinsGA
XM_011515019.1:c.1485+268_1485+269delinsGA (CUL7)	XP_011513321.1:n.1485+268_1485+269delinsGA
XM_011515020.1:c.1389+268_1389+269delinsGA (CUL7)	XP_011513322.1:n.1389+268_1389+269delinsGA
XM_005249503.3:c.1389+268_1389+269delinsGA (CUL7)	XP_005249560.1:n.1389+268_1389+269delinsGA
XM_006715285.2:c.1329+268_1329+269delinsGA (CUL7)	XP_006715348.1:n.1329+268_1329+269delinsGA
XM_011515019.2:c.1485+268_1485+269delinsGA (CUL7)	XP_011513321.1:n.1485+268_1485+269delinsGA
XM_011515020.2:c.1389+268_1389+269delinsGA (CUL7)	XP_011513322.1:n.1389+268_1389+269delinsGA
XM_017011533.1:c.1485+268_1485+269delinsGA (CUL7)	XP_016867022.1:n.1485+268_1485+269delinsGA
XM_017011534.1:c.1485+268_1485+269delinsGA (CUL7)	XP_016867023.1:n.1485+268_1485+269delinsGA
XM_017011535.1:c.1389+268_1389+269delinsGA (CUL7)	XP_016867024.1:n.1389+268_1389+269delinsGA
XM_017011536.2:c.1329+268_1329+269delinsGA (CUL7)	XP_016867025.1:n.1329+268_1329+269delinsGA
XM_017011537.2:c.1329+268_1329+269delinsGA (CUL7)	XP_016867026.1:n.1329+268_1329+269delinsGA
XM_017011538.2:c.1233+268_1233+269delinsGA (CUL7)	XP_016867027.1:n.1233+268_1233+269delinsGA
XM_017011539.2:c.1233+268_1233+269delinsGA (CUL7)	XP_016867028.1:n.1233+268_1233+269delinsGA
XM_017011540.1:c.1485+268_1485+269delinsGA (CUL7)	XP_016867029.1:n.1485+268_1485+269delinsGA
NM_001168370.2:c.1329+268_1329+269delinsGA (CUL7)	NP_001161842.2:n.1329+268_1329+269delinsGA
NM_001374872.1:c.1329+268_1329+269delinsGA (CUL7)	NP_001361801.1:n.1329+268_1329+269delinsGA
NM_001374873.1:c.1233+268_1233+269delinsGA (CUL7)	NP_001361802.1:n.1233+268_1233+269delinsGA
NM_001374874.1:c.1233+268_1233+269delinsGA (CUL7)	NP_001361803.1:n.1233+268_1233+269delinsGA
NM_014780.5:c.1233+268_1233+269delinsGA (CUL7) MANE Select	NP_055595.2:n.1233+268_1233+269delinsGA