Canonical Allele Identifier: CA450369556

Gene: CUL7 KLC4

Linked Data

• gnomAD v4: 6-43043077-C-T
• MyVariant Identifiers: chr6:g.43010815C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043077C>T , CM000668.2:g.43043077C>T	GRCh38
NC_000006.11:g.43010815C>T , CM000668.1:g.43010815C>T	GRCh37
NC_000006.10:g.43118793C>T	NCBI36
NG_016205.1:g.15869G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1530G>A (CUL7)
ENST00000674112.2:c.3459G>A (CUL7)	ENSP00000501166.2:p.Lys1153=
ENST00000685042.1:c.*115G>A (CUL7)	ENSP00000509871.1:n.*115G>A
ENST00000686442.1:n.4020G>A (CUL7)
ENST00000687225.1:c.*1756G>A (CUL7)	ENSP00000509364.1:n.*1756G>A
ENST00000688302.1:n.3742G>A (CUL7)
ENST00000689256.1:n.4036G>A (CUL7)
ENST00000690231.1:c.3459G>A (CUL7)	ENSP00000508461.1:p.Lys1153=
ENST00000265348.9:c.3459G>A (CUL7) MANE Select	ENSP00000265348.4:p.Lys1153=
ENST00000673725.1:c.1408G>A (CUL7)
ENST00000673753.1:n.4298G>A (CUL7)
ENST00000674100.1:c.3555G>A (CUL7)	ENSP00000501292.1:p.Lys1185=
ENST00000674112.1:c.1951G>A (CUL7)
ENST00000674134.1:c.3555G>A (CUL7)	ENSP00000501068.1:p.Lys1185=
ENST00000265348.7:c.3459G>A (CUL7)	ENSP00000265348.3:p.Lys1153=
ENST00000467906.5:c.-984C>T (KLC4)	ENSP00000418759.1:n.-984C>T
ENST00000535468.1:c.3711G>A (CUL7)	ENSP00000438788.1:p.Lys1237=
NM_001168370.1:c.3711G>A (CUL7)	NP_001161842.1:p.Lys1237=
NM_014780.4:c.3459G>A (CUL7)	NP_055595.2:p.Lys1153=
XM_005249503.1:c.3615G>A (CUL7)	XP_005249560.1:p.Lys1205=
XM_006715285.1:c.3555G>A (CUL7)	XP_006715348.1:p.Lys1185=
XM_011515019.1:c.3711G>A (CUL7)	XP_011513321.1:p.Lys1237=
XM_011515020.1:c.3615G>A (CUL7)	XP_011513322.1:p.Lys1205=
XM_011515021.1:c.1320G>A (CUL7)	XP_011513323.1:p.Lys440=
XM_005249503.3:c.3615G>A (CUL7)	XP_005249560.1:p.Lys1205=
XM_006715285.2:c.3555G>A (CUL7)	XP_006715348.1:p.Lys1185=
XM_011515019.2:c.3711G>A (CUL7)	XP_011513321.1:p.Lys1237=
XM_011515020.2:c.3615G>A (CUL7)	XP_011513322.1:p.Lys1205=
XM_017011533.1:c.3738G>A (CUL7)	XP_016867022.1:p.Lys1246=
XM_017011534.1:c.3738G>A (CUL7)	XP_016867023.1:p.Lys1246=
XM_017011535.1:c.3642G>A (CUL7)	XP_016867024.1:p.Lys1214=
XM_017011536.2:c.3582G>A (CUL7)	XP_016867025.1:p.Lys1194=
XM_017011537.2:c.3555G>A (CUL7)	XP_016867026.1:p.Lys1185=
XM_017011538.2:c.3486G>A (CUL7)	XP_016867027.1:p.Lys1162=
XM_017011539.2:c.3459G>A (CUL7)	XP_016867028.1:p.Lys1153=
NM_001168370.2:c.3555G>A (CUL7)	NP_001161842.2:p.Lys1185=
NM_001374872.1:c.3555G>A (CUL7)	NP_001361801.1:p.Lys1185=
NM_001374873.1:c.3459G>A (CUL7)	NP_001361802.1:p.Lys1153=
NM_001374874.1:c.3456G>A (CUL7)	NP_001361803.1:p.Lys1152=
NM_014780.5:c.3459G>A (CUL7) MANE Select	NP_055595.2:p.Lys1153=