Canonical Allele Identifier: CA364203217

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43010822A>G (hg19) ; chr6:g.43043084A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043084A>G , CM000668.2:g.43043084A>G	GRCh38
NC_000006.11:g.43010822A>G , CM000668.1:g.43010822A>G	GRCh37
NC_000006.10:g.43118800A>G	NCBI36
NG_016205.1:g.15862T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1523T>C (CUL7)
ENST00000674112.2:c.3452T>C (CUL7)	ENSP00000501166.2:p.Val1151Ala
ENST00000685042.1:c.*108T>C (CUL7)	ENSP00000509871.1:n.*108T>C
ENST00000686442.1:n.4013T>C (CUL7)
ENST00000687225.1:c.*1749T>C (CUL7)	ENSP00000509364.1:n.*1749T>C
ENST00000688302.1:n.3735T>C (CUL7)
ENST00000689256.1:n.4029T>C (CUL7)
ENST00000690231.1:c.3452T>C (CUL7)	ENSP00000508461.1:p.Val1151Ala
ENST00000265348.9:c.3452T>C (CUL7) MANE Select	ENSP00000265348.4:p.Val1151Ala
ENST00000673725.1:c.1401T>C (CUL7)
ENST00000673753.1:n.4291T>C (CUL7)
ENST00000674100.1:c.3548T>C (CUL7)	ENSP00000501292.1:p.Val1183Ala
ENST00000674112.1:c.1944T>C (CUL7)
ENST00000674134.1:c.3548T>C (CUL7)	ENSP00000501068.1:p.Val1183Ala
ENST00000265348.7:c.3452T>C (CUL7)	ENSP00000265348.3:p.Val1151Ala
ENST00000467906.5:c.-977A>G (KLC4)	ENSP00000418759.1:n.-977A>G
ENST00000535468.1:c.3704T>C (CUL7)	ENSP00000438788.1:p.Val1235Ala
NM_001168370.1:c.3704T>C (CUL7)	NP_001161842.1:p.Val1235Ala
NM_014780.4:c.3452T>C (CUL7)	NP_055595.2:p.Val1151Ala
XM_005249503.1:c.3608T>C (CUL7)	XP_005249560.1:p.Val1203Ala
XM_006715285.1:c.3548T>C (CUL7)	XP_006715348.1:p.Val1183Ala
XM_011515019.1:c.3704T>C (CUL7)	XP_011513321.1:p.Val1235Ala
XM_011515020.1:c.3608T>C (CUL7)	XP_011513322.1:p.Val1203Ala
XM_011515021.1:c.1313T>C (CUL7)	XP_011513323.1:p.Val438Ala
XM_005249503.3:c.3608T>C (CUL7)	XP_005249560.1:p.Val1203Ala
XM_006715285.2:c.3548T>C (CUL7)	XP_006715348.1:p.Val1183Ala
XM_011515019.2:c.3704T>C (CUL7)	XP_011513321.1:p.Val1235Ala
XM_011515020.2:c.3608T>C (CUL7)	XP_011513322.1:p.Val1203Ala
XM_017011533.1:c.3731T>C (CUL7)	XP_016867022.1:p.Val1244Ala
XM_017011534.1:c.3731T>C (CUL7)	XP_016867023.1:p.Val1244Ala
XM_017011535.1:c.3635T>C (CUL7)	XP_016867024.1:p.Val1212Ala
XM_017011536.2:c.3575T>C (CUL7)	XP_016867025.1:p.Val1192Ala
XM_017011537.2:c.3548T>C (CUL7)	XP_016867026.1:p.Val1183Ala
XM_017011538.2:c.3479T>C (CUL7)	XP_016867027.1:p.Val1160Ala
XM_017011539.2:c.3452T>C (CUL7)	XP_016867028.1:p.Val1151Ala
NM_001168370.2:c.3548T>C (CUL7)	NP_001161842.2:p.Val1183Ala
NM_001374872.1:c.3548T>C (CUL7)	NP_001361801.1:p.Val1183Ala
NM_001374873.1:c.3452T>C (CUL7)	NP_001361802.1:p.Val1151Ala
NM_001374874.1:c.3449T>C (CUL7)	NP_001361803.1:p.Val1150Ala
NM_014780.5:c.3452T>C (CUL7) MANE Select	NP_055595.2:p.Val1151Ala