Canonical Allele Identifier: CA138244666

Gene: CUL7 KLC4

Linked Data

• dbSNP Id: rs959529000
• gnomAD v2: 6-43010687-A-G
• gnomAD v4: 6-43042949-A-G
• MyVariant Identifiers: chr6:g.43010687A>G (hg19) ; chr6:g.43042949A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042949A>G , CM000668.2:g.43042949A>G	GRCh38
NC_000006.11:g.43010687A>G , CM000668.1:g.43010687A>G	GRCh37
NC_000006.10:g.43118665A>G	NCBI36
NG_016205.1:g.15997T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1569T>C (CUL7)
ENST00000674112.2:c.3498T>C (CUL7)	ENSP00000501166.2:p.Asp1166=
ENST00000685042.1:c.*154T>C (CUL7)	ENSP00000509871.1:n.*154T>C
ENST00000686442.1:n.4059T>C (CUL7)
ENST00000687225.1:c.*1795T>C (CUL7)	ENSP00000509364.1:n.*1795T>C
ENST00000688302.1:n.3781T>C (CUL7)
ENST00000689256.1:n.4075T>C (CUL7)
ENST00000690231.1:c.3498T>C (CUL7)	ENSP00000508461.1:p.Asp1166=
ENST00000265348.9:c.3498T>C (CUL7) MANE Select	ENSP00000265348.4:p.Asp1166=
ENST00000673725.1:c.1412-43T>C (CUL7)
ENST00000673753.1:n.4337T>C (CUL7)
ENST00000674100.1:c.3594T>C (CUL7)	ENSP00000501292.1:p.Asp1198=
ENST00000674112.1:c.1990T>C (CUL7)
ENST00000674134.1:c.3594T>C (CUL7)	ENSP00000501068.1:p.Asp1198=
ENST00000265348.7:c.3498T>C (CUL7)	ENSP00000265348.3:p.Asp1166=
ENST00000467906.5:c.-1003-109A>G (KLC4)	ENSP00000418759.1:n.-1003-109A>G
ENST00000535468.1:c.3750T>C (CUL7)	ENSP00000438788.1:p.Asp1250=
NM_001168370.1:c.3750T>C (CUL7)	NP_001161842.1:p.Asp1250=
NM_014780.4:c.3498T>C (CUL7)	NP_055595.2:p.Asp1166=
XM_005249503.1:c.3654T>C (CUL7)	XP_005249560.1:p.Asp1218=
XM_006715285.1:c.3594T>C (CUL7)	XP_006715348.1:p.Asp1198=
XM_011515019.1:c.3750T>C (CUL7)	XP_011513321.1:p.Asp1250=
XM_011515020.1:c.3654T>C (CUL7)	XP_011513322.1:p.Asp1218=
XM_011515021.1:c.1359T>C (CUL7)	XP_011513323.1:p.Asp453=
XM_005249503.3:c.3654T>C (CUL7)	XP_005249560.1:p.Asp1218=
XM_006715285.2:c.3594T>C (CUL7)	XP_006715348.1:p.Asp1198=
XM_011515019.2:c.3750T>C (CUL7)	XP_011513321.1:p.Asp1250=
XM_011515020.2:c.3654T>C (CUL7)	XP_011513322.1:p.Asp1218=
XM_017011533.1:c.3777T>C (CUL7)	XP_016867022.1:p.Asp1259=
XM_017011534.1:c.3777T>C (CUL7)	XP_016867023.1:p.Asp1259=
XM_017011535.1:c.3681T>C (CUL7)	XP_016867024.1:p.Asp1227=
XM_017011536.2:c.3621T>C (CUL7)	XP_016867025.1:p.Asp1207=
XM_017011537.2:c.3594T>C (CUL7)	XP_016867026.1:p.Asp1198=
XM_017011538.2:c.3525T>C (CUL7)	XP_016867027.1:p.Asp1175=
XM_017011539.2:c.3498T>C (CUL7)	XP_016867028.1:p.Asp1166=
NM_001168370.2:c.3594T>C (CUL7)	NP_001161842.2:p.Asp1198=
NM_001374872.1:c.3594T>C (CUL7)	NP_001361801.1:p.Asp1198=
NM_001374873.1:c.3498T>C (CUL7)	NP_001361802.1:p.Asp1166=
NM_001374874.1:c.3495T>C (CUL7)	NP_001361803.1:p.Asp1165=
NM_014780.5:c.3498T>C (CUL7) MANE Select	NP_055595.2:p.Asp1166=