Canonical Allele Identifier: CA1624354844

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43042828T= , CM000668.2:g.43042828T= GRCh38
NC_000006.11:g.43010566T= , CM000668.1:g.43010566T= GRCh37
NC_000006.10:g.43118544T= NCBI36
NG_016205.1:g.16118A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478630.2:n.1690A= (CUL7)
ENST00000674112.2:c.3619A= (CUL7) ENSP00000501166.2:p.Lys1207=
ENST00000685042.1:c.*275A= (CUL7) ENSP00000509871.1:n.*275A=
ENST00000686442.1:n.4180A= (CUL7)
ENST00000687225.1:c.*1916A= (CUL7) ENSP00000509364.1:n.*1916A=
ENST00000688302.1:n.3902A= (CUL7)
ENST00000689256.1:n.4196A= (CUL7)
ENST00000690231.1:c.3619A= (CUL7) ENSP00000508461.1:p.Lys1207=
ENST00000265348.9:c.3619A= (CUL7) MANE Select ENSP00000265348.4:p.Lys1207=
ENST00000673725.1:c.1490A= (CUL7)
ENST00000673753.1:n.4458A= (CUL7)
ENST00000674100.1:c.3715A= (CUL7) ENSP00000501292.1:p.Lys1239=
ENST00000674112.1:c.2111A= (CUL7)
ENST00000674134.1:c.3715A= (CUL7) ENSP00000501068.1:p.Lys1239=
ENST00000265348.7:c.3619A= (CUL7) ENSP00000265348.3:p.Lys1207=
ENST00000467906.5:c.-1003-230T= (KLC4) ENSP00000418759.1:n.-1003-230T=
ENST00000535468.1:c.3871A= (CUL7) ENSP00000438788.1:p.Lys1291=
NM_001168370.1:c.3871A= (CUL7) NP_001161842.1:p.Lys1291=
NM_014780.4:c.3619A= (CUL7) NP_055595.2:p.Lys1207=
XM_005249503.1:c.3775A= (CUL7) XP_005249560.1:p.Lys1259=
XM_006715285.1:c.3715A= (CUL7) XP_006715348.1:p.Lys1239=
XM_011515019.1:c.3871A= (CUL7) XP_011513321.1:p.Lys1291=
XM_011515020.1:c.3775A= (CUL7) XP_011513322.1:p.Lys1259=
XM_011515021.1:c.1480A= (CUL7) XP_011513323.1:p.Lys494=
XM_005249503.3:c.3775A= (CUL7) XP_005249560.1:p.Lys1259=
XM_006715285.2:c.3715A= (CUL7) XP_006715348.1:p.Lys1239=
XM_011515019.2:c.3871A= (CUL7) XP_011513321.1:p.Lys1291=
XM_011515020.2:c.3775A= (CUL7) XP_011513322.1:p.Lys1259=
XM_017011533.1:c.3898A= (CUL7) XP_016867022.1:p.Lys1300=
XM_017011534.1:c.3898A= (CUL7) XP_016867023.1:p.Lys1300=
XM_017011535.1:c.3802A= (CUL7) XP_016867024.1:p.Lys1268=
XM_017011536.2:c.3742A= (CUL7) XP_016867025.1:p.Lys1248=
XM_017011537.2:c.3715A= (CUL7) XP_016867026.1:p.Lys1239=
XM_017011538.2:c.3646A= (CUL7) XP_016867027.1:p.Lys1216=
XM_017011539.2:c.3619A= (CUL7) XP_016867028.1:p.Lys1207=
NM_001168370.2:c.3715A= (CUL7) NP_001161842.2:p.Lys1239=
NM_001374872.1:c.3715A= (CUL7) NP_001361801.1:p.Lys1239=
NM_001374873.1:c.3619A= (CUL7) NP_001361802.1:p.Lys1207=
NM_001374874.1:c.3616A= (CUL7) NP_001361803.1:p.Lys1206=
NM_014780.5:c.3619A= (CUL7) MANE Select NP_055595.2:p.Lys1207=