Canonical Allele Identifier: CA364202637

Gene: CUL7 KLC4

Linked Data

• gnomAD v4: 6-43042861-C-T
• MyVariant Identifiers: chr6:g.43010599C>T (hg19) ; chr6:g.43042861C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042861C>T , CM000668.2:g.43042861C>T	GRCh38
NC_000006.11:g.43010599C>T , CM000668.1:g.43010599C>T	GRCh37
NC_000006.10:g.43118577C>T	NCBI36
NG_016205.1:g.16085G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000478630.2:n.1657G>A (CUL7)
ENST00000674112.2:c.3586G>A (CUL7)	ENSP00000501166.2:p.Ala1196Thr
ENST00000685042.1:c.*242G>A (CUL7)	ENSP00000509871.1:n.*242G>A
ENST00000686442.1:n.4147G>A (CUL7)
ENST00000687225.1:c.*1883G>A (CUL7)	ENSP00000509364.1:n.*1883G>A
ENST00000688302.1:n.3869G>A (CUL7)
ENST00000689256.1:n.4163G>A (CUL7)
ENST00000690231.1:c.3586G>A (CUL7)	ENSP00000508461.1:p.Ala1196Thr
ENST00000265348.9:c.3586G>A (CUL7) MANE Select	ENSP00000265348.4:p.Ala1196Thr
ENST00000673725.1:c.1457G>A (CUL7)
ENST00000673753.1:n.4425G>A (CUL7)
ENST00000674100.1:c.3682G>A (CUL7)	ENSP00000501292.1:p.Ala1228Thr
ENST00000674112.1:c.2078G>A (CUL7)
ENST00000674134.1:c.3682G>A (CUL7)	ENSP00000501068.1:p.Ala1228Thr
ENST00000265348.7:c.3586G>A (CUL7)	ENSP00000265348.3:p.Ala1196Thr
ENST00000467906.5:c.-1003-197C>T (KLC4)	ENSP00000418759.1:n.-1003-197C>T
ENST00000535468.1:c.3838G>A (CUL7)	ENSP00000438788.1:p.Ala1280Thr
NM_001168370.1:c.3838G>A (CUL7)	NP_001161842.1:p.Ala1280Thr
NM_014780.4:c.3586G>A (CUL7)	NP_055595.2:p.Ala1196Thr
XM_005249503.1:c.3742G>A (CUL7)	XP_005249560.1:p.Ala1248Thr
XM_006715285.1:c.3682G>A (CUL7)	XP_006715348.1:p.Ala1228Thr
XM_011515019.1:c.3838G>A (CUL7)	XP_011513321.1:p.Ala1280Thr
XM_011515020.1:c.3742G>A (CUL7)	XP_011513322.1:p.Ala1248Thr
XM_011515021.1:c.1447G>A (CUL7)	XP_011513323.1:p.Ala483Thr
XM_005249503.3:c.3742G>A (CUL7)	XP_005249560.1:p.Ala1248Thr
XM_006715285.2:c.3682G>A (CUL7)	XP_006715348.1:p.Ala1228Thr
XM_011515019.2:c.3838G>A (CUL7)	XP_011513321.1:p.Ala1280Thr
XM_011515020.2:c.3742G>A (CUL7)	XP_011513322.1:p.Ala1248Thr
XM_017011533.1:c.3865G>A (CUL7)	XP_016867022.1:p.Ala1289Thr
XM_017011534.1:c.3865G>A (CUL7)	XP_016867023.1:p.Ala1289Thr
XM_017011535.1:c.3769G>A (CUL7)	XP_016867024.1:p.Ala1257Thr
XM_017011536.2:c.3709G>A (CUL7)	XP_016867025.1:p.Ala1237Thr
XM_017011537.2:c.3682G>A (CUL7)	XP_016867026.1:p.Ala1228Thr
XM_017011538.2:c.3613G>A (CUL7)	XP_016867027.1:p.Ala1205Thr
XM_017011539.2:c.3586G>A (CUL7)	XP_016867028.1:p.Ala1196Thr
NM_001168370.2:c.3682G>A (CUL7)	NP_001161842.2:p.Ala1228Thr
NM_001374872.1:c.3682G>A (CUL7)	NP_001361801.1:p.Ala1228Thr
NM_001374873.1:c.3586G>A (CUL7)	NP_001361802.1:p.Ala1196Thr
NM_001374874.1:c.3583G>A (CUL7)	NP_001361803.1:p.Ala1195Thr
NM_014780.5:c.3586G>A (CUL7) MANE Select	NP_055595.2:p.Ala1196Thr