Canonical Allele Identifier: CA364203535

Linked Data

dbSNP Id: rs763304938

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43043138C>A , CM000668.2:g.43043138C>A GRCh38
NC_000006.11:g.43010876C>A , CM000668.1:g.43010876C>A GRCh37
NC_000006.10:g.43118854C>A NCBI36
NG_016205.1:g.15808G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478630.2:n.1469G>T (CUL7)
ENST00000674112.2:c.3398G>T (CUL7) ENSP00000501166.2:p.Arg1133Leu
ENST00000685042.1:c.*54G>T (CUL7) ENSP00000509871.1:n.*54G>T
ENST00000686442.1:n.3959G>T (CUL7)
ENST00000687225.1:c.*1695G>T (CUL7) ENSP00000509364.1:n.*1695G>T
ENST00000688302.1:n.3681G>T (CUL7)
ENST00000689256.1:n.3975G>T (CUL7)
ENST00000690231.1:c.3398G>T (CUL7) ENSP00000508461.1:p.Arg1133Leu
ENST00000265348.9:c.3398G>T (CUL7) MANE Select ENSP00000265348.4:p.Arg1133Leu
ENST00000673725.1:c.1347G>T (CUL7)
ENST00000673753.1:n.4237G>T (CUL7)
ENST00000674100.1:c.3494G>T (CUL7) ENSP00000501292.1:p.Arg1165Leu
ENST00000674112.1:c.1890G>T (CUL7)
ENST00000674134.1:c.3494G>T (CUL7) ENSP00000501068.1:p.Arg1165Leu
ENST00000265348.7:c.3398G>T (CUL7) ENSP00000265348.3:p.Arg1133Leu
ENST00000467906.5:c.-923C>A (KLC4) ENSP00000418759.1:n.-923C>A
ENST00000535468.1:c.3650G>T (CUL7) ENSP00000438788.1:p.Arg1217Leu
NM_001168370.1:c.3650G>T (CUL7) NP_001161842.1:p.Arg1217Leu
NM_014780.4:c.3398G>T (CUL7) NP_055595.2:p.Arg1133Leu
XM_005249503.1:c.3554G>T (CUL7) XP_005249560.1:p.Arg1185Leu
XM_006715285.1:c.3494G>T (CUL7) XP_006715348.1:p.Arg1165Leu
XM_011515019.1:c.3650G>T (CUL7) XP_011513321.1:p.Arg1217Leu
XM_011515020.1:c.3554G>T (CUL7) XP_011513322.1:p.Arg1185Leu
XM_011515021.1:c.1259G>T (CUL7) XP_011513323.1:p.Arg420Leu
XM_005249503.3:c.3554G>T (CUL7) XP_005249560.1:p.Arg1185Leu
XM_006715285.2:c.3494G>T (CUL7) XP_006715348.1:p.Arg1165Leu
XM_011515019.2:c.3650G>T (CUL7) XP_011513321.1:p.Arg1217Leu
XM_011515020.2:c.3554G>T (CUL7) XP_011513322.1:p.Arg1185Leu
XM_017011533.1:c.3677G>T (CUL7) XP_016867022.1:p.Arg1226Leu
XM_017011534.1:c.3677G>T (CUL7) XP_016867023.1:p.Arg1226Leu
XM_017011535.1:c.3581G>T (CUL7) XP_016867024.1:p.Arg1194Leu
XM_017011536.2:c.3521G>T (CUL7) XP_016867025.1:p.Arg1174Leu
XM_017011537.2:c.3494G>T (CUL7) XP_016867026.1:p.Arg1165Leu
XM_017011538.2:c.3425G>T (CUL7) XP_016867027.1:p.Arg1142Leu
XM_017011539.2:c.3398G>T (CUL7) XP_016867028.1:p.Arg1133Leu
NM_001168370.2:c.3494G>T (CUL7) NP_001161842.2:p.Arg1165Leu
NM_001374872.1:c.3494G>T (CUL7) NP_001361801.1:p.Arg1165Leu
NM_001374873.1:c.3398G>T (CUL7) NP_001361802.1:p.Arg1133Leu
NM_001374874.1:c.3395G>T (CUL7) NP_001361803.1:p.Arg1132Leu
NM_014780.5:c.3398G>T (CUL7) MANE Select NP_055595.2:p.Arg1133Leu