Canonical Allele Identifier: CA1624354860

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042863A= , CM000668.2:g.43042863A=	GRCh38
NC_000006.11:g.43010601A= , CM000668.1:g.43010601A=	GRCh37
NC_000006.10:g.43118579A=	NCBI36
NG_016205.1:g.16083T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000478630.2:n.1655T= (CUL7)
ENST00000674112.2:c.3584T= (CUL7)	ENSP00000501166.2:p.Leu1195=
ENST00000685042.1:c.*240T= (CUL7)	ENSP00000509871.1:n.*240T=
ENST00000686442.1:n.4145T= (CUL7)
ENST00000687225.1:c.*1881T= (CUL7)	ENSP00000509364.1:n.*1881T=
ENST00000688302.1:n.3867T= (CUL7)
ENST00000689256.1:n.4161T= (CUL7)
ENST00000690231.1:c.3584T= (CUL7)	ENSP00000508461.1:p.Leu1195=
ENST00000265348.9:c.3584T= (CUL7) MANE Select	ENSP00000265348.4:p.Leu1195=
ENST00000673725.1:c.1455T= (CUL7)
ENST00000673753.1:n.4423T= (CUL7)
ENST00000674100.1:c.3680T= (CUL7)	ENSP00000501292.1:p.Leu1227=
ENST00000674112.1:c.2076T= (CUL7)
ENST00000674134.1:c.3680T= (CUL7)	ENSP00000501068.1:p.Leu1227=
ENST00000265348.7:c.3584T= (CUL7)	ENSP00000265348.3:p.Leu1195=
ENST00000467906.5:c.-1003-195A= (KLC4)	ENSP00000418759.1:n.-1003-195A=
ENST00000535468.1:c.3836T= (CUL7)	ENSP00000438788.1:p.Leu1279=
NM_001168370.1:c.3836T= (CUL7)	NP_001161842.1:p.Leu1279=
NM_014780.4:c.3584T= (CUL7)	NP_055595.2:p.Leu1195=
XM_005249503.1:c.3740T= (CUL7)	XP_005249560.1:p.Leu1247=
XM_006715285.1:c.3680T= (CUL7)	XP_006715348.1:p.Leu1227=
XM_011515019.1:c.3836T= (CUL7)	XP_011513321.1:p.Leu1279=
XM_011515020.1:c.3740T= (CUL7)	XP_011513322.1:p.Leu1247=
XM_011515021.1:c.1445T= (CUL7)	XP_011513323.1:p.Leu482=
XM_005249503.3:c.3740T= (CUL7)	XP_005249560.1:p.Leu1247=
XM_006715285.2:c.3680T= (CUL7)	XP_006715348.1:p.Leu1227=
XM_011515019.2:c.3836T= (CUL7)	XP_011513321.1:p.Leu1279=
XM_011515020.2:c.3740T= (CUL7)	XP_011513322.1:p.Leu1247=
XM_017011533.1:c.3863T= (CUL7)	XP_016867022.1:p.Leu1288=
XM_017011534.1:c.3863T= (CUL7)	XP_016867023.1:p.Leu1288=
XM_017011535.1:c.3767T= (CUL7)	XP_016867024.1:p.Leu1256=
XM_017011536.2:c.3707T= (CUL7)	XP_016867025.1:p.Leu1236=
XM_017011537.2:c.3680T= (CUL7)	XP_016867026.1:p.Leu1227=
XM_017011538.2:c.3611T= (CUL7)	XP_016867027.1:p.Leu1204=
XM_017011539.2:c.3584T= (CUL7)	XP_016867028.1:p.Leu1195=
NM_001168370.2:c.3680T= (CUL7)	NP_001161842.2:p.Leu1227=
NM_001374872.1:c.3680T= (CUL7)	NP_001361801.1:p.Leu1227=
NM_001374873.1:c.3584T= (CUL7)	NP_001361802.1:p.Leu1195=
NM_001374874.1:c.3581T= (CUL7)	NP_001361803.1:p.Leu1194=
NM_014780.5:c.3584T= (CUL7) MANE Select	NP_055595.2:p.Leu1195=