Canonical Allele Identifier: CA1624354981

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043160C= , CM000668.2:g.43043160C=	GRCh38
NC_000006.11:g.43010898C= , CM000668.1:g.43010898C=	GRCh37
NC_000006.10:g.43118876C=	NCBI36
NG_016205.1:g.15786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1447G= (CUL7)
ENST00000674112.2:c.3376G= (CUL7)	ENSP00000501166.2:p.Asp1126=
ENST00000685042.1:c.*32G= (CUL7)	ENSP00000509871.1:n.*32G=
ENST00000686442.1:n.3937G= (CUL7)
ENST00000687225.1:c.*1673G= (CUL7)	ENSP00000509364.1:n.*1673G=
ENST00000688302.1:n.3659G= (CUL7)
ENST00000689256.1:n.3953G= (CUL7)
ENST00000690231.1:c.3376G= (CUL7)	ENSP00000508461.1:p.Asp1126=
ENST00000265348.9:c.3376G= (CUL7) MANE Select	ENSP00000265348.4:p.Asp1126=
ENST00000673725.1:c.1325G= (CUL7)
ENST00000673753.1:n.4215G= (CUL7)
ENST00000674100.1:c.3472G= (CUL7)	ENSP00000501292.1:p.Asp1158=
ENST00000674112.1:c.1868G= (CUL7)
ENST00000674134.1:c.3472G= (CUL7)	ENSP00000501068.1:p.Asp1158=
ENST00000265348.7:c.3376G= (CUL7)	ENSP00000265348.3:p.Asp1126=
ENST00000467906.5:c.-901C= (KLC4)	ENSP00000418759.1:n.-901C=
ENST00000535468.1:c.3628G= (CUL7)	ENSP00000438788.1:p.Asp1210=
NM_001168370.1:c.3628G= (CUL7)	NP_001161842.1:p.Asp1210=
NM_014780.4:c.3376G= (CUL7)	NP_055595.2:p.Asp1126=
XM_005249503.1:c.3532G= (CUL7)	XP_005249560.1:p.Asp1178=
XM_006715285.1:c.3472G= (CUL7)	XP_006715348.1:p.Asp1158=
XM_011515019.1:c.3628G= (CUL7)	XP_011513321.1:p.Asp1210=
XM_011515020.1:c.3532G= (CUL7)	XP_011513322.1:p.Asp1178=
XM_011515021.1:c.1237G= (CUL7)	XP_011513323.1:p.Asp413=
XM_005249503.3:c.3532G= (CUL7)	XP_005249560.1:p.Asp1178=
XM_006715285.2:c.3472G= (CUL7)	XP_006715348.1:p.Asp1158=
XM_011515019.2:c.3628G= (CUL7)	XP_011513321.1:p.Asp1210=
XM_011515020.2:c.3532G= (CUL7)	XP_011513322.1:p.Asp1178=
XM_017011533.1:c.3655G= (CUL7)	XP_016867022.1:p.Asp1219=
XM_017011534.1:c.3655G= (CUL7)	XP_016867023.1:p.Asp1219=
XM_017011535.1:c.3559G= (CUL7)	XP_016867024.1:p.Asp1187=
XM_017011536.2:c.3499G= (CUL7)	XP_016867025.1:p.Asp1167=
XM_017011537.2:c.3472G= (CUL7)	XP_016867026.1:p.Asp1158=
XM_017011538.2:c.3403G= (CUL7)	XP_016867027.1:p.Asp1135=
XM_017011539.2:c.3376G= (CUL7)	XP_016867028.1:p.Asp1126=
NM_001168370.2:c.3472G= (CUL7)	NP_001161842.2:p.Asp1158=
NM_001374872.1:c.3472G= (CUL7)	NP_001361801.1:p.Asp1158=
NM_001374873.1:c.3376G= (CUL7)	NP_001361802.1:p.Asp1126=
NM_001374874.1:c.3373G= (CUL7)	NP_001361803.1:p.Asp1125=
NM_014780.5:c.3376G= (CUL7) MANE Select	NP_055595.2:p.Asp1126=