Canonical Allele Identifier: CA1624354817

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042770_43042771delinsGA , CM000668.2:g.43042770_43042771delinsGA	GRCh38
NC_000006.11:g.43010508_43010509delinsGA , CM000668.1:g.43010508_43010509delinsGA	GRCh37
NC_000006.10:g.43118486_43118487delinsGA	NCBI36
NG_016205.1:g.16175_16176delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1716+31_1716+32delinsTC (CUL7)
ENST00000674112.2:c.3645+31_3645+32delinsTC (CUL7)	ENSP00000501166.2:n.3645+31_3645+32delinsTC
ENST00000685042.1:c.*301+31_*301+32delinsTC (CUL7)	ENSP00000509871.1:n.*301+31_*301+32delinsTC
ENST00000686442.1:n.4206+31_4206+32delinsTC (CUL7)
ENST00000687225.1:c.*1942+31_*1942+32delinsTC (CUL7)	ENSP00000509364.1:n.*1942+31_*1942+32delinsTC
ENST00000688302.1:n.3928+31_3928+32delinsTC (CUL7)
ENST00000689256.1:n.4222+31_4222+32delinsTC (CUL7)
ENST00000690231.1:c.3645+31_3645+32delinsTC (CUL7)	ENSP00000508461.1:n.3645+31_3645+32delinsTC
ENST00000265348.9:c.3645+31_3645+32delinsTC (CUL7) MANE Select	ENSP00000265348.4:n.3645+31_3645+32delinsTC
ENST00000673725.1:c.1516+31_1516+32delinsTC (CUL7)
ENST00000673753.1:n.4484+31_4484+32delinsTC (CUL7)
ENST00000674100.1:c.3741+31_3741+32delinsTC (CUL7)	ENSP00000501292.1:n.3741+31_3741+32delinsTC
ENST00000674112.1:c.2137+31_2137+32delinsTC (CUL7)
ENST00000674134.1:c.3741+31_3741+32delinsTC (CUL7)	ENSP00000501068.1:n.3741+31_3741+32delinsTC
ENST00000265348.7:c.3645+31_3645+32delinsTC (CUL7)	ENSP00000265348.3:n.3645+31_3645+32delinsTC
ENST00000467906.5:c.-1003-288_-1003-287delinsGA (KLC4)	ENSP00000418759.1:n.-1003-288_-1003-287delinsGA
ENST00000535468.1:c.3897+31_3897+32delinsTC (CUL7)	ENSP00000438788.1:n.3897+31_3897+32delinsTC
NM_001168370.1:c.3897+31_3897+32delinsTC (CUL7)	NP_001161842.1:n.3897+31_3897+32delinsTC
NM_014780.4:c.3645+31_3645+32delinsTC (CUL7)	NP_055595.2:n.3645+31_3645+32delinsTC
XM_005249503.1:c.3801+31_3801+32delinsTC (CUL7)	XP_005249560.1:n.3801+31_3801+32delinsTC
XM_006715285.1:c.3741+31_3741+32delinsTC (CUL7)	XP_006715348.1:n.3741+31_3741+32delinsTC
XM_011515019.1:c.3897+31_3897+32delinsTC (CUL7)	XP_011513321.1:n.3897+31_3897+32delinsTC
XM_011515020.1:c.3801+31_3801+32delinsTC (CUL7)	XP_011513322.1:n.3801+31_3801+32delinsTC
XM_011515021.1:c.1506+31_1506+32delinsTC (CUL7)	XP_011513323.1:n.1506+31_1506+32delinsTC
XM_005249503.3:c.3801+31_3801+32delinsTC (CUL7)	XP_005249560.1:n.3801+31_3801+32delinsTC
XM_006715285.2:c.3741+31_3741+32delinsTC (CUL7)	XP_006715348.1:n.3741+31_3741+32delinsTC
XM_011515019.2:c.3897+31_3897+32delinsTC (CUL7)	XP_011513321.1:n.3897+31_3897+32delinsTC
XM_011515020.2:c.3801+31_3801+32delinsTC (CUL7)	XP_011513322.1:n.3801+31_3801+32delinsTC
XM_017011533.1:c.3924+31_3924+32delinsTC (CUL7)	XP_016867022.1:n.3924+31_3924+32delinsTC
XM_017011534.1:c.3924+31_3924+32delinsTC (CUL7)	XP_016867023.1:n.3924+31_3924+32delinsTC
XM_017011535.1:c.3828+31_3828+32delinsTC (CUL7)	XP_016867024.1:n.3828+31_3828+32delinsTC
XM_017011536.2:c.3768+31_3768+32delinsTC (CUL7)	XP_016867025.1:n.3768+31_3768+32delinsTC
XM_017011537.2:c.3741+31_3741+32delinsTC (CUL7)	XP_016867026.1:n.3741+31_3741+32delinsTC
XM_017011538.2:c.3672+31_3672+32delinsTC (CUL7)	XP_016867027.1:n.3672+31_3672+32delinsTC
XM_017011539.2:c.3645+31_3645+32delinsTC (CUL7)	XP_016867028.1:n.3645+31_3645+32delinsTC
NM_001168370.2:c.3741+31_3741+32delinsTC (CUL7)	NP_001161842.2:n.3741+31_3741+32delinsTC
NM_001374872.1:c.3741+31_3741+32delinsTC (CUL7)	NP_001361801.1:n.3741+31_3741+32delinsTC
NM_001374873.1:c.3645+31_3645+32delinsTC (CUL7)	NP_001361802.1:n.3645+31_3645+32delinsTC
NM_001374874.1:c.3642+31_3642+32delinsTC (CUL7)	NP_001361803.1:n.3642+31_3642+32delinsTC
NM_014780.5:c.3645+31_3645+32delinsTC (CUL7) MANE Select	NP_055595.2:n.3645+31_3645+32delinsTC