Canonical Allele Identifier: CA364202342

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43010548C>T (hg19) ; chr6:g.43042810C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042810C>T , CM000668.2:g.43042810C>T	GRCh38
NC_000006.11:g.43010548C>T , CM000668.1:g.43010548C>T	GRCh37
NC_000006.10:g.43118526C>T	NCBI36
NG_016205.1:g.16136G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1708G>A (CUL7)
ENST00000674112.2:c.3637G>A (CUL7)	ENSP00000501166.2:p.Ala1213Thr
ENST00000685042.1:c.*293G>A (CUL7)	ENSP00000509871.1:n.*293G>A
ENST00000686442.1:n.4198G>A (CUL7)
ENST00000687225.1:c.*1934G>A (CUL7)	ENSP00000509364.1:n.*1934G>A
ENST00000688302.1:n.3920G>A (CUL7)
ENST00000689256.1:n.4214G>A (CUL7)
ENST00000690231.1:c.3637G>A (CUL7)	ENSP00000508461.1:p.Ala1213Thr
ENST00000265348.9:c.3637G>A (CUL7) MANE Select	ENSP00000265348.4:p.Ala1213Thr
ENST00000673725.1:c.1508G>A (CUL7)
ENST00000673753.1:n.4476G>A (CUL7)
ENST00000674100.1:c.3733G>A (CUL7)	ENSP00000501292.1:p.Ala1245Thr
ENST00000674112.1:c.2129G>A (CUL7)
ENST00000674134.1:c.3733G>A (CUL7)	ENSP00000501068.1:p.Ala1245Thr
ENST00000265348.7:c.3637G>A (CUL7)	ENSP00000265348.3:p.Ala1213Thr
ENST00000467906.5:c.-1003-248C>T (KLC4)	ENSP00000418759.1:n.-1003-248C>T
ENST00000535468.1:c.3889G>A (CUL7)	ENSP00000438788.1:p.Ala1297Thr
NM_001168370.1:c.3889G>A (CUL7)	NP_001161842.1:p.Ala1297Thr
NM_014780.4:c.3637G>A (CUL7)	NP_055595.2:p.Ala1213Thr
XM_005249503.1:c.3793G>A (CUL7)	XP_005249560.1:p.Ala1265Thr
XM_006715285.1:c.3733G>A (CUL7)	XP_006715348.1:p.Ala1245Thr
XM_011515019.1:c.3889G>A (CUL7)	XP_011513321.1:p.Ala1297Thr
XM_011515020.1:c.3793G>A (CUL7)	XP_011513322.1:p.Ala1265Thr
XM_011515021.1:c.1498G>A (CUL7)	XP_011513323.1:p.Ala500Thr
XM_005249503.3:c.3793G>A (CUL7)	XP_005249560.1:p.Ala1265Thr
XM_006715285.2:c.3733G>A (CUL7)	XP_006715348.1:p.Ala1245Thr
XM_011515019.2:c.3889G>A (CUL7)	XP_011513321.1:p.Ala1297Thr
XM_011515020.2:c.3793G>A (CUL7)	XP_011513322.1:p.Ala1265Thr
XM_017011533.1:c.3916G>A (CUL7)	XP_016867022.1:p.Ala1306Thr
XM_017011534.1:c.3916G>A (CUL7)	XP_016867023.1:p.Ala1306Thr
XM_017011535.1:c.3820G>A (CUL7)	XP_016867024.1:p.Ala1274Thr
XM_017011536.2:c.3760G>A (CUL7)	XP_016867025.1:p.Ala1254Thr
XM_017011537.2:c.3733G>A (CUL7)	XP_016867026.1:p.Ala1245Thr
XM_017011538.2:c.3664G>A (CUL7)	XP_016867027.1:p.Ala1222Thr
XM_017011539.2:c.3637G>A (CUL7)	XP_016867028.1:p.Ala1213Thr
NM_001168370.2:c.3733G>A (CUL7)	NP_001161842.2:p.Ala1245Thr
NM_001374872.1:c.3733G>A (CUL7)	NP_001361801.1:p.Ala1245Thr
NM_001374873.1:c.3637G>A (CUL7)	NP_001361802.1:p.Ala1213Thr
NM_001374874.1:c.3634G>A (CUL7)	NP_001361803.1:p.Ala1212Thr
NM_014780.5:c.3637G>A (CUL7) MANE Select	NP_055595.2:p.Ala1213Thr