Canonical Allele Identifier: CA364203616

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43043151A>C , CM000668.2:g.43043151A>C GRCh38
NC_000006.11:g.43010889A>C , CM000668.1:g.43010889A>C GRCh37
NC_000006.10:g.43118867A>C NCBI36
NG_016205.1:g.15795T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000478630.2:n.1456T>G (CUL7)
ENST00000674112.2:c.3385T>G (CUL7) ENSP00000501166.2:p.Ser1129Ala
ENST00000685042.1:c.*41T>G (CUL7) ENSP00000509871.1:n.*41T>G
ENST00000686442.1:n.3946T>G (CUL7)
ENST00000687225.1:c.*1682T>G (CUL7) ENSP00000509364.1:n.*1682T>G
ENST00000688302.1:n.3668T>G (CUL7)
ENST00000689256.1:n.3962T>G (CUL7)
ENST00000690231.1:c.3385T>G (CUL7) ENSP00000508461.1:p.Ser1129Ala
ENST00000265348.9:c.3385T>G (CUL7) MANE Select ENSP00000265348.4:p.Ser1129Ala
ENST00000673725.1:c.1334T>G (CUL7)
ENST00000673753.1:n.4224T>G (CUL7)
ENST00000674100.1:c.3481T>G (CUL7) ENSP00000501292.1:p.Ser1161Ala
ENST00000674112.1:c.1877T>G (CUL7)
ENST00000674134.1:c.3481T>G (CUL7) ENSP00000501068.1:p.Ser1161Ala
ENST00000265348.7:c.3385T>G (CUL7) ENSP00000265348.3:p.Ser1129Ala
ENST00000467906.5:c.-910A>C (KLC4) ENSP00000418759.1:n.-910A>C
ENST00000535468.1:c.3637T>G (CUL7) ENSP00000438788.1:p.Ser1213Ala
NM_001168370.1:c.3637T>G (CUL7) NP_001161842.1:p.Ser1213Ala
NM_014780.4:c.3385T>G (CUL7) NP_055595.2:p.Ser1129Ala
XM_005249503.1:c.3541T>G (CUL7) XP_005249560.1:p.Ser1181Ala
XM_006715285.1:c.3481T>G (CUL7) XP_006715348.1:p.Ser1161Ala
XM_011515019.1:c.3637T>G (CUL7) XP_011513321.1:p.Ser1213Ala
XM_011515020.1:c.3541T>G (CUL7) XP_011513322.1:p.Ser1181Ala
XM_011515021.1:c.1246T>G (CUL7) XP_011513323.1:p.Ser416Ala
XM_005249503.3:c.3541T>G (CUL7) XP_005249560.1:p.Ser1181Ala
XM_006715285.2:c.3481T>G (CUL7) XP_006715348.1:p.Ser1161Ala
XM_011515019.2:c.3637T>G (CUL7) XP_011513321.1:p.Ser1213Ala
XM_011515020.2:c.3541T>G (CUL7) XP_011513322.1:p.Ser1181Ala
XM_017011533.1:c.3664T>G (CUL7) XP_016867022.1:p.Ser1222Ala
XM_017011534.1:c.3664T>G (CUL7) XP_016867023.1:p.Ser1222Ala
XM_017011535.1:c.3568T>G (CUL7) XP_016867024.1:p.Ser1190Ala
XM_017011536.2:c.3508T>G (CUL7) XP_016867025.1:p.Ser1170Ala
XM_017011537.2:c.3481T>G (CUL7) XP_016867026.1:p.Ser1161Ala
XM_017011538.2:c.3412T>G (CUL7) XP_016867027.1:p.Ser1138Ala
XM_017011539.2:c.3385T>G (CUL7) XP_016867028.1:p.Ser1129Ala
NM_001168370.2:c.3481T>G (CUL7) NP_001161842.2:p.Ser1161Ala
NM_001374872.1:c.3481T>G (CUL7) NP_001361801.1:p.Ser1161Ala
NM_001374873.1:c.3385T>G (CUL7) NP_001361802.1:p.Ser1129Ala
NM_001374874.1:c.3382T>G (CUL7) NP_001361803.1:p.Ser1128Ala
NM_014780.5:c.3385T>G (CUL7) MANE Select NP_055595.2:p.Ser1129Ala