Canonical Allele Identifier: CA450369664

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43010913T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043175T>G , CM000668.2:g.43043175T>G	GRCh38
NC_000006.11:g.43010913T>G , CM000668.1:g.43010913T>G	GRCh37
NC_000006.10:g.43118891T>G	NCBI36
NG_016205.1:g.15771A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1432A>C (CUL7)
ENST00000674112.2:c.3361A>C (CUL7)	ENSP00000501166.2:p.Arg1121=
ENST00000685042.1:c.*17A>C (CUL7)	ENSP00000509871.1:n.*17A>C
ENST00000686442.1:n.3922A>C (CUL7)
ENST00000687225.1:c.*1658A>C (CUL7)	ENSP00000509364.1:n.*1658A>C
ENST00000688302.1:n.3644A>C (CUL7)
ENST00000689256.1:n.3938A>C (CUL7)
ENST00000690231.1:c.3361A>C (CUL7)	ENSP00000508461.1:p.Arg1121=
ENST00000265348.9:c.3361A>C (CUL7) MANE Select	ENSP00000265348.4:p.Arg1121=
ENST00000673725.1:c.1310A>C (CUL7)
ENST00000673753.1:n.4200A>C (CUL7)
ENST00000674100.1:c.3457A>C (CUL7)	ENSP00000501292.1:p.Arg1153=
ENST00000674112.1:c.1853A>C (CUL7)
ENST00000674134.1:c.3457A>C (CUL7)	ENSP00000501068.1:p.Arg1153=
ENST00000265348.7:c.3361A>C (CUL7)	ENSP00000265348.3:p.Arg1121=
ENST00000467906.5:c.-886T>G (KLC4)	ENSP00000418759.1:n.-886T>G
ENST00000535468.1:c.3613A>C (CUL7)	ENSP00000438788.1:p.Arg1205=
NM_001168370.1:c.3613A>C (CUL7)	NP_001161842.1:p.Arg1205=
NM_014780.4:c.3361A>C (CUL7)	NP_055595.2:p.Arg1121=
XM_005249503.1:c.3517A>C (CUL7)	XP_005249560.1:p.Arg1173=
XM_006715285.1:c.3457A>C (CUL7)	XP_006715348.1:p.Arg1153=
XM_011515019.1:c.3613A>C (CUL7)	XP_011513321.1:p.Arg1205=
XM_011515020.1:c.3517A>C (CUL7)	XP_011513322.1:p.Arg1173=
XM_011515021.1:c.1222A>C (CUL7)	XP_011513323.1:p.Arg408=
XM_005249503.3:c.3517A>C (CUL7)	XP_005249560.1:p.Arg1173=
XM_006715285.2:c.3457A>C (CUL7)	XP_006715348.1:p.Arg1153=
XM_011515019.2:c.3613A>C (CUL7)	XP_011513321.1:p.Arg1205=
XM_011515020.2:c.3517A>C (CUL7)	XP_011513322.1:p.Arg1173=
XM_017011533.1:c.3640A>C (CUL7)	XP_016867022.1:p.Arg1214=
XM_017011534.1:c.3640A>C (CUL7)	XP_016867023.1:p.Arg1214=
XM_017011535.1:c.3544A>C (CUL7)	XP_016867024.1:p.Arg1182=
XM_017011536.2:c.3484A>C (CUL7)	XP_016867025.1:p.Arg1162=
XM_017011537.2:c.3457A>C (CUL7)	XP_016867026.1:p.Arg1153=
XM_017011538.2:c.3388A>C (CUL7)	XP_016867027.1:p.Arg1130=
XM_017011539.2:c.3361A>C (CUL7)	XP_016867028.1:p.Arg1121=
NM_001168370.2:c.3457A>C (CUL7)	NP_001161842.2:p.Arg1153=
NM_001374872.1:c.3457A>C (CUL7)	NP_001361801.1:p.Arg1153=
NM_001374873.1:c.3361A>C (CUL7)	NP_001361802.1:p.Arg1121=
NM_001374874.1:c.3358A>C (CUL7)	NP_001361803.1:p.Arg1120=
NM_014780.5:c.3361A>C (CUL7) MANE Select	NP_055595.2:p.Arg1121=