Canonical Allele Identifier: CA2678806015

Gene: CUL7 KLC4

Linked Data

• gnomAD v4: 6-43042740-GAGGTGAGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042744_43042752del , CM000668.2:g.43042744_43042752del	GRCh38
NC_000006.11:g.43010482_43010490del , CM000668.1:g.43010482_43010490del	GRCh37
NC_000006.10:g.43118460_43118468del	NCBI36
NG_016205.1:g.16197_16205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1716+53_1716+61del (CUL7)
ENST00000674112.2:c.3645+53_3645+61del (CUL7)	ENSP00000501166.2:n.3645+53_3645+61del
ENST00000685042.1:c.*301+53_*301+61del (CUL7)	ENSP00000509871.1:n.*301+53_*301+61del
ENST00000686442.1:n.4206+53_4206+61del (CUL7)
ENST00000687225.1:c.*1942+53_*1942+61del (CUL7)	ENSP00000509364.1:n.*1942+53_*1942+61del
ENST00000688302.1:n.3928+53_3928+61del (CUL7)
ENST00000689256.1:n.4222+53_4222+61del (CUL7)
ENST00000690231.1:c.3645+53_3645+61del (CUL7)	ENSP00000508461.1:n.3645+53_3645+61del
ENST00000265348.9:c.3645+53_3645+61del (CUL7) MANE Select	ENSP00000265348.4:n.3645+53_3645+61del
ENST00000673725.1:c.1516+53_1516+61del (CUL7)
ENST00000673753.1:n.4484+53_4484+61del (CUL7)
ENST00000674100.1:c.3741+53_3741+61del (CUL7)	ENSP00000501292.1:n.3741+53_3741+61del
ENST00000674112.1:c.2137+53_2137+61del (CUL7)
ENST00000674134.1:c.3741+53_3741+61del (CUL7)	ENSP00000501068.1:n.3741+53_3741+61del
ENST00000265348.7:c.3645+53_3645+61del (CUL7)	ENSP00000265348.3:n.3645+53_3645+61del
ENST00000467906.5:c.-1003-314_-1003-306del (KLC4)	ENSP00000418759.1:n.-1003-314_-1003-306del
ENST00000535468.1:c.3897+53_3897+61del (CUL7)	ENSP00000438788.1:n.3897+53_3897+61del
NM_001168370.1:c.3897+53_3897+61del (CUL7)	NP_001161842.1:n.3897+53_3897+61del
NM_014780.4:c.3645+53_3645+61del (CUL7)	NP_055595.2:n.3645+53_3645+61del
XM_005249503.1:c.3801+53_3801+61del (CUL7)	XP_005249560.1:n.3801+53_3801+61del
XM_006715285.1:c.3741+53_3741+61del (CUL7)	XP_006715348.1:n.3741+53_3741+61del
XM_011515019.1:c.3897+53_3897+61del (CUL7)	XP_011513321.1:n.3897+53_3897+61del
XM_011515020.1:c.3801+53_3801+61del (CUL7)	XP_011513322.1:n.3801+53_3801+61del
XM_011515021.1:c.1506+53_1506+61del (CUL7)	XP_011513323.1:n.1506+53_1506+61del
XM_005249503.3:c.3801+53_3801+61del (CUL7)	XP_005249560.1:n.3801+53_3801+61del
XM_006715285.2:c.3741+53_3741+61del (CUL7)	XP_006715348.1:n.3741+53_3741+61del
XM_011515019.2:c.3897+53_3897+61del (CUL7)	XP_011513321.1:n.3897+53_3897+61del
XM_011515020.2:c.3801+53_3801+61del (CUL7)	XP_011513322.1:n.3801+53_3801+61del
XM_017011533.1:c.3924+53_3924+61del (CUL7)	XP_016867022.1:n.3924+53_3924+61del
XM_017011534.1:c.3924+53_3924+61del (CUL7)	XP_016867023.1:n.3924+53_3924+61del
XM_017011535.1:c.3828+53_3828+61del (CUL7)	XP_016867024.1:n.3828+53_3828+61del
XM_017011536.2:c.3768+53_3768+61del (CUL7)	XP_016867025.1:n.3768+53_3768+61del
XM_017011537.2:c.3741+53_3741+61del (CUL7)	XP_016867026.1:n.3741+53_3741+61del
XM_017011538.2:c.3672+53_3672+61del (CUL7)	XP_016867027.1:n.3672+53_3672+61del
XM_017011539.2:c.3645+53_3645+61del (CUL7)	XP_016867028.1:n.3645+53_3645+61del
NM_001168370.2:c.3741+53_3741+61del (CUL7)	NP_001161842.2:n.3741+53_3741+61del
NM_001374872.1:c.3741+53_3741+61del (CUL7)	NP_001361801.1:n.3741+53_3741+61del
NM_001374873.1:c.3645+53_3645+61del (CUL7)	NP_001361802.1:n.3645+53_3645+61del
NM_001374874.1:c.3642+53_3642+61del (CUL7)	NP_001361803.1:n.3642+53_3642+61del
NM_014780.5:c.3645+53_3645+61del (CUL7) MANE Select	NP_055595.2:n.3645+53_3645+61del