Canonical Allele Identifier: CA364203216

Gene: CUL7 KLC4

Linked Data

• dbSNP Id: rs1581921023
• MyVariant Identifiers: chr6:g.43010822A>C (hg19) ; chr6:g.43043084A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1523T>G (CUL7)
ENST00000674112.2:c.3452T>G (CUL7)	ENSP00000501166.2:p.Val1151Gly
ENST00000685042.1:c.*108T>G (CUL7)	ENSP00000509871.1:n.*108T>G
ENST00000686442.1:n.4013T>G (CUL7)
ENST00000687225.1:c.*1749T>G (CUL7)	ENSP00000509364.1:n.*1749T>G
ENST00000688302.1:n.3735T>G (CUL7)
ENST00000689256.1:n.4029T>G (CUL7)
ENST00000690231.1:c.3452T>G (CUL7)	ENSP00000508461.1:p.Val1151Gly
ENST00000265348.9:c.3452T>G (CUL7) MANE Select	ENSP00000265348.4:p.Val1151Gly
ENST00000673725.1:c.1401T>G (CUL7)
ENST00000673753.1:n.4291T>G (CUL7)
ENST00000674100.1:c.3548T>G (CUL7)	ENSP00000501292.1:p.Val1183Gly
ENST00000674112.1:c.1944T>G (CUL7)
ENST00000674134.1:c.3548T>G (CUL7)	ENSP00000501068.1:p.Val1183Gly
ENST00000265348.7:c.3452T>G (CUL7)	ENSP00000265348.3:p.Val1151Gly
ENST00000467906.5:c.-977A>C (KLC4)	ENSP00000418759.1:n.-977A>C
ENST00000535468.1:c.3704T>G (CUL7)	ENSP00000438788.1:p.Val1235Gly
NM_001168370.1:c.3704T>G (CUL7)	NP_001161842.1:p.Val1235Gly
NM_014780.4:c.3452T>G (CUL7)	NP_055595.2:p.Val1151Gly
XM_005249503.1:c.3608T>G (CUL7)	XP_005249560.1:p.Val1203Gly
XM_006715285.1:c.3548T>G (CUL7)	XP_006715348.1:p.Val1183Gly
XM_011515019.1:c.3704T>G (CUL7)	XP_011513321.1:p.Val1235Gly
XM_011515020.1:c.3608T>G (CUL7)	XP_011513322.1:p.Val1203Gly
XM_011515021.1:c.1313T>G (CUL7)	XP_011513323.1:p.Val438Gly
XM_005249503.3:c.3608T>G (CUL7)	XP_005249560.1:p.Val1203Gly
XM_006715285.2:c.3548T>G (CUL7)	XP_006715348.1:p.Val1183Gly
XM_011515019.2:c.3704T>G (CUL7)	XP_011513321.1:p.Val1235Gly
XM_011515020.2:c.3608T>G (CUL7)	XP_011513322.1:p.Val1203Gly
XM_017011533.1:c.3731T>G (CUL7)	XP_016867022.1:p.Val1244Gly
XM_017011534.1:c.3731T>G (CUL7)	XP_016867023.1:p.Val1244Gly
XM_017011535.1:c.3635T>G (CUL7)	XP_016867024.1:p.Val1212Gly
XM_017011536.2:c.3575T>G (CUL7)	XP_016867025.1:p.Val1192Gly
XM_017011537.2:c.3548T>G (CUL7)	XP_016867026.1:p.Val1183Gly
XM_017011538.2:c.3479T>G (CUL7)	XP_016867027.1:p.Val1160Gly
XM_017011539.2:c.3452T>G (CUL7)	XP_016867028.1:p.Val1151Gly
NM_001168370.2:c.3548T>G (CUL7)	NP_001161842.2:p.Val1183Gly
NM_001374872.1:c.3548T>G (CUL7)	NP_001361801.1:p.Val1183Gly
NM_001374873.1:c.3452T>G (CUL7)	NP_001361802.1:p.Val1151Gly
NM_001374874.1:c.3449T>G (CUL7)	NP_001361803.1:p.Val1150Gly
NM_014780.5:c.3452T>G (CUL7) MANE Select	NP_055595.2:p.Val1151Gly