Canonical Allele Identifier: CA364203704

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43043162T>A , CM000668.2:g.43043162T>A GRCh38
NC_000006.11:g.43010900T>A , CM000668.1:g.43010900T>A GRCh37
NC_000006.10:g.43118878T>A NCBI36
NG_016205.1:g.15784A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478630.2:n.1445A>T (CUL7)
ENST00000674112.2:c.3374A>T (CUL7) ENSP00000501166.2:p.His1125Leu
ENST00000685042.1:c.*30A>T (CUL7) ENSP00000509871.1:n.*30A>T
ENST00000686442.1:n.3935A>T (CUL7)
ENST00000687225.1:c.*1671A>T (CUL7) ENSP00000509364.1:n.*1671A>T
ENST00000688302.1:n.3657A>T (CUL7)
ENST00000689256.1:n.3951A>T (CUL7)
ENST00000690231.1:c.3374A>T (CUL7) ENSP00000508461.1:p.His1125Leu
ENST00000265348.9:c.3374A>T (CUL7) MANE Select ENSP00000265348.4:p.His1125Leu
ENST00000673725.1:c.1323A>T (CUL7)
ENST00000673753.1:n.4213A>T (CUL7)
ENST00000674100.1:c.3470A>T (CUL7) ENSP00000501292.1:p.His1157Leu
ENST00000674112.1:c.1866A>T (CUL7)
ENST00000674134.1:c.3470A>T (CUL7) ENSP00000501068.1:p.His1157Leu
ENST00000265348.7:c.3374A>T (CUL7) ENSP00000265348.3:p.His1125Leu
ENST00000467906.5:c.-899T>A (KLC4) ENSP00000418759.1:n.-899T>A
ENST00000535468.1:c.3626A>T (CUL7) ENSP00000438788.1:p.His1209Leu
NM_001168370.1:c.3626A>T (CUL7) NP_001161842.1:p.His1209Leu
NM_014780.4:c.3374A>T (CUL7) NP_055595.2:p.His1125Leu
XM_005249503.1:c.3530A>T (CUL7) XP_005249560.1:p.His1177Leu
XM_006715285.1:c.3470A>T (CUL7) XP_006715348.1:p.His1157Leu
XM_011515019.1:c.3626A>T (CUL7) XP_011513321.1:p.His1209Leu
XM_011515020.1:c.3530A>T (CUL7) XP_011513322.1:p.His1177Leu
XM_011515021.1:c.1235A>T (CUL7) XP_011513323.1:p.His412Leu
XM_005249503.3:c.3530A>T (CUL7) XP_005249560.1:p.His1177Leu
XM_006715285.2:c.3470A>T (CUL7) XP_006715348.1:p.His1157Leu
XM_011515019.2:c.3626A>T (CUL7) XP_011513321.1:p.His1209Leu
XM_011515020.2:c.3530A>T (CUL7) XP_011513322.1:p.His1177Leu
XM_017011533.1:c.3653A>T (CUL7) XP_016867022.1:p.His1218Leu
XM_017011534.1:c.3653A>T (CUL7) XP_016867023.1:p.His1218Leu
XM_017011535.1:c.3557A>T (CUL7) XP_016867024.1:p.His1186Leu
XM_017011536.2:c.3497A>T (CUL7) XP_016867025.1:p.His1166Leu
XM_017011537.2:c.3470A>T (CUL7) XP_016867026.1:p.His1157Leu
XM_017011538.2:c.3401A>T (CUL7) XP_016867027.1:p.His1134Leu
XM_017011539.2:c.3374A>T (CUL7) XP_016867028.1:p.His1125Leu
NM_001168370.2:c.3470A>T (CUL7) NP_001161842.2:p.His1157Leu
NM_001374872.1:c.3470A>T (CUL7) NP_001361801.1:p.His1157Leu
NM_001374873.1:c.3374A>T (CUL7) NP_001361802.1:p.His1125Leu
NM_001374874.1:c.3371A>T (CUL7) NP_001361803.1:p.His1124Leu
NM_014780.5:c.3374A>T (CUL7) MANE Select NP_055595.2:p.His1125Leu