Canonical Allele Identifier: CA138244629

Gene: CUL7 KLC4

Linked Data

• ClinVar Variation Id: 1444856
• ClinVar RCV Id: RCV001956007 ; RCV002562904
• dbSNP Id: rs902734461
• gnomAD v2: 6-43010617-G-A
• gnomAD v3: 6-43042879-G-A
• gnomAD v4: 6-43042879-G-A
• MyVariant Identifiers: chr6:g.43010617G>A (hg19) ; chr6:g.43042879G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042879G>A , CM000668.2:g.43042879G>A	GRCh38
NC_000006.11:g.43010617G>A , CM000668.1:g.43010617G>A	GRCh37
NC_000006.10:g.43118595G>A	NCBI36
NG_016205.1:g.16067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1639C>T (CUL7)
ENST00000674112.2:c.3568C>T (CUL7)	ENSP00000501166.2:p.Arg1190Trp
ENST00000685042.1:c.*224C>T (CUL7)	ENSP00000509871.1:n.*224C>T
ENST00000686442.1:n.4129C>T (CUL7)
ENST00000687225.1:c.*1865C>T (CUL7)	ENSP00000509364.1:n.*1865C>T
ENST00000688302.1:n.3851C>T (CUL7)
ENST00000689256.1:n.4145C>T (CUL7)
ENST00000690231.1:c.3568C>T (CUL7)	ENSP00000508461.1:p.Arg1190Trp
ENST00000265348.9:c.3568C>T (CUL7) MANE Select	ENSP00000265348.4:p.Arg1190Trp
ENST00000673725.1:c.1439C>T (CUL7)
ENST00000673753.1:n.4407C>T (CUL7)
ENST00000674100.1:c.3664C>T (CUL7)	ENSP00000501292.1:p.Arg1222Trp
ENST00000674112.1:c.2060C>T (CUL7)
ENST00000674134.1:c.3664C>T (CUL7)	ENSP00000501068.1:p.Arg1222Trp
ENST00000265348.7:c.3568C>T (CUL7)	ENSP00000265348.3:p.Arg1190Trp
ENST00000467906.5:c.-1003-179G>A (KLC4)	ENSP00000418759.1:n.-1003-179G>A
ENST00000535468.1:c.3820C>T (CUL7)	ENSP00000438788.1:p.Arg1274Trp
NM_001168370.1:c.3820C>T (CUL7)	NP_001161842.1:p.Arg1274Trp
NM_014780.4:c.3568C>T (CUL7)	NP_055595.2:p.Arg1190Trp
XM_005249503.1:c.3724C>T (CUL7)	XP_005249560.1:p.Arg1242Trp
XM_006715285.1:c.3664C>T (CUL7)	XP_006715348.1:p.Arg1222Trp
XM_011515019.1:c.3820C>T (CUL7)	XP_011513321.1:p.Arg1274Trp
XM_011515020.1:c.3724C>T (CUL7)	XP_011513322.1:p.Arg1242Trp
XM_011515021.1:c.1429C>T (CUL7)	XP_011513323.1:p.Arg477Trp
XM_005249503.3:c.3724C>T (CUL7)	XP_005249560.1:p.Arg1242Trp
XM_006715285.2:c.3664C>T (CUL7)	XP_006715348.1:p.Arg1222Trp
XM_011515019.2:c.3820C>T (CUL7)	XP_011513321.1:p.Arg1274Trp
XM_011515020.2:c.3724C>T (CUL7)	XP_011513322.1:p.Arg1242Trp
XM_017011533.1:c.3847C>T (CUL7)	XP_016867022.1:p.Arg1283Trp
XM_017011534.1:c.3847C>T (CUL7)	XP_016867023.1:p.Arg1283Trp
XM_017011535.1:c.3751C>T (CUL7)	XP_016867024.1:p.Arg1251Trp
XM_017011536.2:c.3691C>T (CUL7)	XP_016867025.1:p.Arg1231Trp
XM_017011537.2:c.3664C>T (CUL7)	XP_016867026.1:p.Arg1222Trp
XM_017011538.2:c.3595C>T (CUL7)	XP_016867027.1:p.Arg1199Trp
XM_017011539.2:c.3568C>T (CUL7)	XP_016867028.1:p.Arg1190Trp
NM_001168370.2:c.3664C>T (CUL7)	NP_001161842.2:p.Arg1222Trp
NM_001374872.1:c.3664C>T (CUL7)	NP_001361801.1:p.Arg1222Trp
NM_001374873.1:c.3568C>T (CUL7)	NP_001361802.1:p.Arg1190Trp
NM_001374874.1:c.3565C>T (CUL7)	NP_001361803.1:p.Arg1189Trp
NM_014780.5:c.3568C>T (CUL7) MANE Select	NP_055595.2:p.Arg1190Trp