Canonical Allele Identifier: CA1624358700

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43051518_43051520delinsCCT , CM000668.2:g.43051518_43051520delinsCCT	GRCh38
NC_000006.11:g.43019256_43019258delinsCCT , CM000668.1:g.43019256_43019258delinsCCT	GRCh37
NC_000006.10:g.43127234_43127236delinsCCT	NCBI36
NG_016205.1:g.7426_7428delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.733-52_733-50delinsAGG (CUL7)	ENSP00000501166.2:n.733-52_733-50delinsAGG
ENST00000683160.1:n.1115-52_1115-50delinsAGG (CUL7)
ENST00000683493.1:n.774-52_774-50delinsAGG (CUL7)
ENST00000685042.1:c.733-52_733-50delinsAGG (CUL7)	ENSP00000509871.1:n.733-52_733-50delinsAGG
ENST00000686442.1:n.1016-52_1016-50delinsAGG (CUL7)
ENST00000687225.1:c.829-52_829-50delinsAGG (CUL7)	ENSP00000509364.1:n.829-52_829-50delinsAGG
ENST00000688302.1:n.1016-52_1016-50delinsAGG (CUL7)
ENST00000688707.1:c.829-52_829-50delinsAGG (CUL7)	ENSP00000510608.1:n.829-52_829-50delinsAGG
ENST00000689256.1:n.1032-52_1032-50delinsAGG (CUL7)
ENST00000690231.1:c.733-52_733-50delinsAGG (CUL7)	ENSP00000508461.1:n.733-52_733-50delinsAGG
ENST00000265348.9:c.733-52_733-50delinsAGG (CUL7) MANE Select	ENSP00000265348.4:n.733-52_733-50delinsAGG
ENST00000673753.1:n.1067-52_1067-50delinsAGG (CUL7)
ENST00000673761.1:c.1470-38_1470-36delinsAGG	ENSP00000501018.1:n.1470-38_1470-36delinsAGG
ENST00000674100.1:c.829-52_829-50delinsAGG (CUL7)	ENSP00000501292.1:n.829-52_829-50delinsAGG
ENST00000674134.1:c.829-52_829-50delinsAGG (CUL7)	ENSP00000501068.1:n.829-52_829-50delinsAGG
ENST00000265348.7:c.733-52_733-50delinsAGG (CUL7)	ENSP00000265348.3:n.733-52_733-50delinsAGG
ENST00000467906.5:c.-552-7508_-552-7506delinsCCT (KLC4)	ENSP00000418759.1:n.-552-7508_-552-7506delinsCCT
ENST00000535468.1:c.985-52_985-50delinsAGG (CUL7)	ENSP00000438788.1:n.985-52_985-50delinsAGG
NM_001168370.1:c.985-52_985-50delinsAGG (CUL7)	NP_001161842.1:n.985-52_985-50delinsAGG
NM_014780.4:c.733-52_733-50delinsAGG (CUL7)	NP_055595.2:n.733-52_733-50delinsAGG
XM_005249503.1:c.889-52_889-50delinsAGG (CUL7)	XP_005249560.1:n.889-52_889-50delinsAGG
XM_006715285.1:c.829-52_829-50delinsAGG (CUL7)	XP_006715348.1:n.829-52_829-50delinsAGG
XM_011515019.1:c.985-52_985-50delinsAGG (CUL7)	XP_011513321.1:n.985-52_985-50delinsAGG
XM_011515020.1:c.889-52_889-50delinsAGG (CUL7)	XP_011513322.1:n.889-52_889-50delinsAGG
XM_005249503.3:c.889-52_889-50delinsAGG (CUL7)	XP_005249560.1:n.889-52_889-50delinsAGG
XM_006715285.2:c.829-52_829-50delinsAGG (CUL7)	XP_006715348.1:n.829-52_829-50delinsAGG
XM_011515019.2:c.985-52_985-50delinsAGG (CUL7)	XP_011513321.1:n.985-52_985-50delinsAGG
XM_011515020.2:c.889-52_889-50delinsAGG (CUL7)	XP_011513322.1:n.889-52_889-50delinsAGG
XM_017011533.1:c.985-52_985-50delinsAGG (CUL7)	XP_016867022.1:n.985-52_985-50delinsAGG
XM_017011534.1:c.985-52_985-50delinsAGG (CUL7)	XP_016867023.1:n.985-52_985-50delinsAGG
XM_017011535.1:c.889-52_889-50delinsAGG (CUL7)	XP_016867024.1:n.889-52_889-50delinsAGG
XM_017011536.2:c.829-52_829-50delinsAGG (CUL7)	XP_016867025.1:n.829-52_829-50delinsAGG
XM_017011537.2:c.829-52_829-50delinsAGG (CUL7)	XP_016867026.1:n.829-52_829-50delinsAGG
XM_017011538.2:c.733-52_733-50delinsAGG (CUL7)	XP_016867027.1:n.733-52_733-50delinsAGG
XM_017011539.2:c.733-52_733-50delinsAGG (CUL7)	XP_016867028.1:n.733-52_733-50delinsAGG
XM_017011540.1:c.985-52_985-50delinsAGG (CUL7)	XP_016867029.1:n.985-52_985-50delinsAGG
NM_001168370.2:c.829-52_829-50delinsAGG (CUL7)	NP_001161842.2:n.829-52_829-50delinsAGG
NM_001374872.1:c.829-52_829-50delinsAGG (CUL7)	NP_001361801.1:n.829-52_829-50delinsAGG
NM_001374873.1:c.733-52_733-50delinsAGG (CUL7)	NP_001361802.1:n.733-52_733-50delinsAGG
NM_001374874.1:c.733-52_733-50delinsAGG (CUL7)	NP_001361803.1:n.733-52_733-50delinsAGG
NM_014780.5:c.733-52_733-50delinsAGG (CUL7) MANE Select	NP_055595.2:n.733-52_733-50delinsAGG