Canonical Allele Identifier: CA3813473

Gene: CUL7 KLC4

Linked Data

• dbSNP Id: rs769724772
• ExAC: 6:43010751 C / T
• gnomAD v2: 6-43010751-C-T
• gnomAD v4: 6-43043013-C-T
• MyVariant Identifiers: chr6:g.43010751C>T (hg19) ; chr6:g.43043013C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043013C>T , CM000668.2:g.43043013C>T	GRCh38
NC_000006.11:g.43010751C>T , CM000668.1:g.43010751C>T	GRCh37
NC_000006.10:g.43118729C>T	NCBI36
NG_016205.1:g.15933G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000478630.2:n.1534-29G>A (CUL7)
ENST00000674112.2:c.3463-29G>A (CUL7)	ENSP00000501166.2:n.3463-29G>A
ENST00000685042.1:c.*119-29G>A (CUL7)	ENSP00000509871.1:n.*119-29G>A
ENST00000686442.1:n.4024-29G>A (CUL7)
ENST00000687225.1:c.*1760-29G>A (CUL7)	ENSP00000509364.1:n.*1760-29G>A
ENST00000688302.1:n.3746-29G>A (CUL7)
ENST00000689256.1:n.4040-29G>A (CUL7)
ENST00000690231.1:c.3463-29G>A (CUL7)	ENSP00000508461.1:n.3463-29G>A
ENST00000265348.9:c.3463-29G>A (CUL7) MANE Select	ENSP00000265348.4:n.3463-29G>A
ENST00000673725.1:c.1411+61G>A (CUL7)
ENST00000673753.1:n.4302-29G>A (CUL7)
ENST00000674100.1:c.3559-29G>A (CUL7)	ENSP00000501292.1:n.3559-29G>A
ENST00000674112.1:c.1955-29G>A (CUL7)
ENST00000674134.1:c.3559-29G>A (CUL7)	ENSP00000501068.1:n.3559-29G>A
ENST00000265348.7:c.3463-29G>A (CUL7)	ENSP00000265348.3:n.3463-29G>A
ENST00000467906.5:c.-1003-45C>T (KLC4)	ENSP00000418759.1:n.-1003-45C>T
ENST00000535468.1:c.3715-29G>A (CUL7)	ENSP00000438788.1:n.3715-29G>A
NM_001168370.1:c.3715-29G>A (CUL7)	NP_001161842.1:n.3715-29G>A
NM_014780.4:c.3463-29G>A (CUL7)	NP_055595.2:n.3463-29G>A
XM_005249503.1:c.3619-29G>A (CUL7)	XP_005249560.1:n.3619-29G>A
XM_006715285.1:c.3559-29G>A (CUL7)	XP_006715348.1:n.3559-29G>A
XM_011515019.1:c.3715-29G>A (CUL7)	XP_011513321.1:n.3715-29G>A
XM_011515020.1:c.3619-29G>A (CUL7)	XP_011513322.1:n.3619-29G>A
XM_011515021.1:c.1324-29G>A (CUL7)	XP_011513323.1:n.1324-29G>A
XM_005249503.3:c.3619-29G>A (CUL7)	XP_005249560.1:n.3619-29G>A
XM_006715285.2:c.3559-29G>A (CUL7)	XP_006715348.1:n.3559-29G>A
XM_011515019.2:c.3715-29G>A (CUL7)	XP_011513321.1:n.3715-29G>A
XM_011515020.2:c.3619-29G>A (CUL7)	XP_011513322.1:n.3619-29G>A
XM_017011533.1:c.3742-29G>A (CUL7)	XP_016867022.1:n.3742-29G>A
XM_017011534.1:c.3742-29G>A (CUL7)	XP_016867023.1:n.3742-29G>A
XM_017011535.1:c.3646-29G>A (CUL7)	XP_016867024.1:n.3646-29G>A
XM_017011536.2:c.3586-29G>A (CUL7)	XP_016867025.1:n.3586-29G>A
XM_017011537.2:c.3559-29G>A (CUL7)	XP_016867026.1:n.3559-29G>A
XM_017011538.2:c.3490-29G>A (CUL7)	XP_016867027.1:n.3490-29G>A
XM_017011539.2:c.3463-29G>A (CUL7)	XP_016867028.1:n.3463-29G>A
NM_001168370.2:c.3559-29G>A (CUL7)	NP_001161842.2:n.3559-29G>A
NM_001374872.1:c.3559-29G>A (CUL7)	NP_001361801.1:n.3559-29G>A
NM_001374873.1:c.3463-29G>A (CUL7)	NP_001361802.1:n.3463-29G>A
NM_001374874.1:c.3460-29G>A (CUL7)	NP_001361803.1:n.3460-29G>A
NM_014780.5:c.3463-29G>A (CUL7) MANE Select	NP_055595.2:n.3463-29G>A