Canonical Allele Identifier: CA364208547

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43013011G>C (hg19) ; chr6:g.43045273G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43045273G>C , CM000668.2:g.43045273G>C	GRCh38
NC_000006.11:g.43013011G>C , CM000668.1:g.43013011G>C	GRCh37
NC_000006.10:g.43120989G>C	NCBI36
NG_016205.1:g.13673C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1063C>G (CUL7)
ENST00000674112.2:c.2992C>G (CUL7)	ENSP00000501166.2:p.Gln998Glu
ENST00000685042.1:c.2992C>G (CUL7)	ENSP00000509871.1:p.Gln998Glu
ENST00000686442.1:n.3553C>G (CUL7)
ENST00000687225.1:c.*1289C>G (CUL7)	ENSP00000509364.1:n.*1289C>G
ENST00000688302.1:n.3275C>G (CUL7)
ENST00000689256.1:n.3569C>G (CUL7)
ENST00000690231.1:c.2992C>G (CUL7)	ENSP00000508461.1:p.Gln998Glu
ENST00000265348.9:c.2992C>G (CUL7) MANE Select	ENSP00000265348.4:p.Gln998Glu
ENST00000673725.1:c.941C>G (CUL7)
ENST00000673753.1:n.3831C>G (CUL7)
ENST00000674100.1:c.3088C>G (CUL7)	ENSP00000501292.1:p.Gln1030Glu
ENST00000674112.1:c.1484C>G (CUL7)
ENST00000674134.1:c.3088C>G (CUL7)	ENSP00000501068.1:p.Gln1030Glu
ENST00000265348.7:c.2992C>G (CUL7)	ENSP00000265348.3:p.Gln998Glu
ENST00000467906.5:c.-553+1765G>C (KLC4)	ENSP00000418759.1:n.-553+1765G>C
ENST00000535468.1:c.3244C>G (CUL7)	ENSP00000438788.1:p.Gln1082Glu
NM_001168370.1:c.3244C>G (CUL7)	NP_001161842.1:p.Gln1082Glu
NM_014780.4:c.2992C>G (CUL7)	NP_055595.2:p.Gln998Glu
XM_005249503.1:c.3148C>G (CUL7)	XP_005249560.1:p.Gln1050Glu
XM_006715285.1:c.3088C>G (CUL7)	XP_006715348.1:p.Gln1030Glu
XM_011515019.1:c.3244C>G (CUL7)	XP_011513321.1:p.Gln1082Glu
XM_011515020.1:c.3148C>G (CUL7)	XP_011513322.1:p.Gln1050Glu
XM_011515021.1:c.853C>G (CUL7)	XP_011513323.1:p.Gln285Glu
XM_005249503.3:c.3148C>G (CUL7)	XP_005249560.1:p.Gln1050Glu
XM_006715285.2:c.3088C>G (CUL7)	XP_006715348.1:p.Gln1030Glu
XM_011515019.2:c.3244C>G (CUL7)	XP_011513321.1:p.Gln1082Glu
XM_011515020.2:c.3148C>G (CUL7)	XP_011513322.1:p.Gln1050Glu
XM_017011533.1:c.3271C>G (CUL7)	XP_016867022.1:p.Gln1091Glu
XM_017011534.1:c.3271C>G (CUL7)	XP_016867023.1:p.Gln1091Glu
XM_017011535.1:c.3175C>G (CUL7)	XP_016867024.1:p.Gln1059Glu
XM_017011536.2:c.3115C>G (CUL7)	XP_016867025.1:p.Gln1039Glu
XM_017011537.2:c.3088C>G (CUL7)	XP_016867026.1:p.Gln1030Glu
XM_017011538.2:c.3019C>G (CUL7)	XP_016867027.1:p.Gln1007Glu
XM_017011539.2:c.2992C>G (CUL7)	XP_016867028.1:p.Gln998Glu
NM_001168370.2:c.3088C>G (CUL7)	NP_001161842.2:p.Gln1030Glu
NM_001374872.1:c.3088C>G (CUL7)	NP_001361801.1:p.Gln1030Glu
NM_001374873.1:c.2992C>G (CUL7)	NP_001361802.1:p.Gln998Glu
NM_001374874.1:c.2992C>G (CUL7)	NP_001361803.1:p.Gln998Glu
NM_014780.5:c.2992C>G (CUL7) MANE Select	NP_055595.2:p.Gln998Glu