Canonical Allele Identifier: CA364203127

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43010712A>C (hg19) ; chr6:g.43042974A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042974A>C , CM000668.2:g.43042974A>C	GRCh38
NC_000006.11:g.43010712A>C , CM000668.1:g.43010712A>C	GRCh37
NC_000006.10:g.43118690A>C	NCBI36
NG_016205.1:g.15972T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000478630.2:n.1544T>G (CUL7)
ENST00000674112.2:c.3473T>G (CUL7)	ENSP00000501166.2:p.Phe1158Cys
ENST00000685042.1:c.*129T>G (CUL7)	ENSP00000509871.1:n.*129T>G
ENST00000686442.1:n.4034T>G (CUL7)
ENST00000687225.1:c.*1770T>G (CUL7)	ENSP00000509364.1:n.*1770T>G
ENST00000688302.1:n.3756T>G (CUL7)
ENST00000689256.1:n.4050T>G (CUL7)
ENST00000690231.1:c.3473T>G (CUL7)	ENSP00000508461.1:p.Phe1158Cys
ENST00000265348.9:c.3473T>G (CUL7) MANE Select	ENSP00000265348.4:p.Phe1158Cys
ENST00000673725.1:c.1412-68T>G (CUL7)
ENST00000673753.1:n.4312T>G (CUL7)
ENST00000674100.1:c.3569T>G (CUL7)	ENSP00000501292.1:p.Phe1190Cys
ENST00000674112.1:c.1965T>G (CUL7)
ENST00000674134.1:c.3569T>G (CUL7)	ENSP00000501068.1:p.Phe1190Cys
ENST00000265348.7:c.3473T>G (CUL7)	ENSP00000265348.3:p.Phe1158Cys
ENST00000467906.5:c.-1003-84A>C (KLC4)	ENSP00000418759.1:n.-1003-84A>C
ENST00000535468.1:c.3725T>G (CUL7)	ENSP00000438788.1:p.Phe1242Cys
NM_001168370.1:c.3725T>G (CUL7)	NP_001161842.1:p.Phe1242Cys
NM_014780.4:c.3473T>G (CUL7)	NP_055595.2:p.Phe1158Cys
XM_005249503.1:c.3629T>G (CUL7)	XP_005249560.1:p.Phe1210Cys
XM_006715285.1:c.3569T>G (CUL7)	XP_006715348.1:p.Phe1190Cys
XM_011515019.1:c.3725T>G (CUL7)	XP_011513321.1:p.Phe1242Cys
XM_011515020.1:c.3629T>G (CUL7)	XP_011513322.1:p.Phe1210Cys
XM_011515021.1:c.1334T>G (CUL7)	XP_011513323.1:p.Phe445Cys
XM_005249503.3:c.3629T>G (CUL7)	XP_005249560.1:p.Phe1210Cys
XM_006715285.2:c.3569T>G (CUL7)	XP_006715348.1:p.Phe1190Cys
XM_011515019.2:c.3725T>G (CUL7)	XP_011513321.1:p.Phe1242Cys
XM_011515020.2:c.3629T>G (CUL7)	XP_011513322.1:p.Phe1210Cys
XM_017011533.1:c.3752T>G (CUL7)	XP_016867022.1:p.Phe1251Cys
XM_017011534.1:c.3752T>G (CUL7)	XP_016867023.1:p.Phe1251Cys
XM_017011535.1:c.3656T>G (CUL7)	XP_016867024.1:p.Phe1219Cys
XM_017011536.2:c.3596T>G (CUL7)	XP_016867025.1:p.Phe1199Cys
XM_017011537.2:c.3569T>G (CUL7)	XP_016867026.1:p.Phe1190Cys
XM_017011538.2:c.3500T>G (CUL7)	XP_016867027.1:p.Phe1167Cys
XM_017011539.2:c.3473T>G (CUL7)	XP_016867028.1:p.Phe1158Cys
NM_001168370.2:c.3569T>G (CUL7)	NP_001161842.2:p.Phe1190Cys
NM_001374872.1:c.3569T>G (CUL7)	NP_001361801.1:p.Phe1190Cys
NM_001374873.1:c.3473T>G (CUL7)	NP_001361802.1:p.Phe1158Cys
NM_001374874.1:c.3470T>G (CUL7)	NP_001361803.1:p.Phe1157Cys
NM_014780.5:c.3473T>G (CUL7) MANE Select	NP_055595.2:p.Phe1158Cys