Canonical Allele Identifier: CA364218688

Gene: CUL7 KLC4

Linked Data

• gnomAD v4: 6-43048251-A-G
• MyVariant Identifiers: chr6:g.43015989A>G (hg19) ; chr6:g.43048251A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43048251A>G , CM000668.2:g.43048251A>G	GRCh38
NC_000006.11:g.43015989A>G , CM000668.1:g.43015989A>G	GRCh37
NC_000006.10:g.43123967A>G	NCBI36
NG_016205.1:g.10695T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.2066T>C (CUL7)	ENSP00000501166.2:p.Ile689Thr
ENST00000685042.1:c.2066T>C (CUL7)	ENSP00000509871.1:p.Ile689Thr
ENST00000686442.1:n.2349T>C (CUL7)
ENST00000687225.1:c.2162T>C (CUL7)	ENSP00000509364.1:p.Ile721Thr
ENST00000688302.1:n.2349T>C (CUL7)
ENST00000689256.1:n.2365T>C (CUL7)
ENST00000690231.1:c.2066T>C (CUL7)	ENSP00000508461.1:p.Ile689Thr
ENST00000265348.9:c.2066T>C (CUL7) MANE Select	ENSP00000265348.4:p.Ile689Thr
ENST00000673725.1:c.15T>C (CUL7)
ENST00000673753.1:n.2400T>C (CUL7)
ENST00000674100.1:c.2162T>C (CUL7)	ENSP00000501292.1:p.Ile721Thr
ENST00000674112.1:c.558T>C (CUL7)
ENST00000674134.1:c.2162T>C (CUL7)	ENSP00000501068.1:p.Ile721Thr
ENST00000265348.7:c.2066T>C (CUL7)	ENSP00000265348.3:p.Ile689Thr
ENST00000467906.5:c.-553+4743A>G (KLC4)	ENSP00000418759.1:n.-553+4743A>G
ENST00000535468.1:c.2318T>C (CUL7)	ENSP00000438788.1:p.Ile773Thr
NM_001168370.1:c.2318T>C (CUL7)	NP_001161842.1:p.Ile773Thr
NM_014780.4:c.2066T>C (CUL7)	NP_055595.2:p.Ile689Thr
XM_005249503.1:c.2222T>C (CUL7)	XP_005249560.1:p.Ile741Thr
XM_006715285.1:c.2162T>C (CUL7)	XP_006715348.1:p.Ile721Thr
XM_011515019.1:c.2318T>C (CUL7)	XP_011513321.1:p.Ile773Thr
XM_011515020.1:c.2222T>C (CUL7)	XP_011513322.1:p.Ile741Thr
XM_011515021.1:c.-117T>C (CUL7)	XP_011513323.1:n.-117T>C
XM_005249503.3:c.2222T>C (CUL7)	XP_005249560.1:p.Ile741Thr
XM_006715285.2:c.2162T>C (CUL7)	XP_006715348.1:p.Ile721Thr
XM_011515019.2:c.2318T>C (CUL7)	XP_011513321.1:p.Ile773Thr
XM_011515020.2:c.2222T>C (CUL7)	XP_011513322.1:p.Ile741Thr
XM_017011533.1:c.2345T>C (CUL7)	XP_016867022.1:p.Ile782Thr
XM_017011534.1:c.2345T>C (CUL7)	XP_016867023.1:p.Ile782Thr
XM_017011535.1:c.2249T>C (CUL7)	XP_016867024.1:p.Ile750Thr
XM_017011536.2:c.2189T>C (CUL7)	XP_016867025.1:p.Ile730Thr
XM_017011537.2:c.2162T>C (CUL7)	XP_016867026.1:p.Ile721Thr
XM_017011538.2:c.2093T>C (CUL7)	XP_016867027.1:p.Ile698Thr
XM_017011539.2:c.2066T>C (CUL7)	XP_016867028.1:p.Ile689Thr
XM_017011540.1:c.2345T>C (CUL7)	XP_016867029.1:p.Ile782Thr
NM_001168370.2:c.2162T>C (CUL7)	NP_001161842.2:p.Ile721Thr
NM_001374872.1:c.2162T>C (CUL7)	NP_001361801.1:p.Ile721Thr
NM_001374873.1:c.2066T>C (CUL7)	NP_001361802.1:p.Ile689Thr
NM_001374874.1:c.2066T>C (CUL7)	NP_001361803.1:p.Ile689Thr
NM_014780.5:c.2066T>C (CUL7) MANE Select	NP_055595.2:p.Ile689Thr