Canonical Allele Identifier: CA2534444111

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43042983_43042984del , CM000668.2:g.43042983_43042984del GRCh38
NC_000006.11:g.43010721_43010722del , CM000668.1:g.43010721_43010722del GRCh37
NC_000006.10:g.43118699_43118700del NCBI36
NG_016205.1:g.15963_15964del

Transcript Alleles

HGVS Amino-acid Change
ENST00000478630.2:n.1535_1536del (CUL7)
ENST00000674112.2:c.3464_3465del (CUL7) ENSP00000501166.2:p.Val1155GlufsTer11
ENST00000685042.1:c.*120_*121del (CUL7) ENSP00000509871.1:n.*120_*121del
ENST00000686442.1:n.4025_4026del (CUL7)
ENST00000687225.1:c.*1761_*1762del (CUL7) ENSP00000509364.1:n.*1761_*1762del
ENST00000688302.1:n.3747_3748del (CUL7)
ENST00000689256.1:n.4041_4042del (CUL7)
ENST00000690231.1:c.3464_3465del (CUL7) ENSP00000508461.1:p.Val1155GlufsTer11
ENST00000265348.9:c.3464_3465del (CUL7) MANE Select ENSP00000265348.4:p.Val1155GlufsTer11
ENST00000673725.1:c.1412-77_1412-76del (CUL7)
ENST00000673753.1:n.4303_4304del (CUL7)
ENST00000674100.1:c.3560_3561del (CUL7) ENSP00000501292.1:p.Val1187GlufsTer11
ENST00000674112.1:c.1956_1957del (CUL7)
ENST00000674134.1:c.3560_3561del (CUL7) ENSP00000501068.1:p.Val1187GlufsTer11
ENST00000265348.7:c.3464_3465del (CUL7) ENSP00000265348.3:p.Val1155GlufsTer11
ENST00000467906.5:c.-1003-75_-1003-74del (KLC4) ENSP00000418759.1:n.-1003-75_-1003-74del
ENST00000535468.1:c.3716_3717del (CUL7) ENSP00000438788.1:p.Val1239GlufsTer11
NM_001168370.1:c.3716_3717del (CUL7) NP_001161842.1:p.Val1239GlufsTer11
NM_014780.4:c.3464_3465del (CUL7) NP_055595.2:p.Val1155GlufsTer11
XM_005249503.1:c.3620_3621del (CUL7) XP_005249560.1:p.Val1207GlufsTer11
XM_006715285.1:c.3560_3561del (CUL7) XP_006715348.1:p.Val1187GlufsTer11
XM_011515019.1:c.3716_3717del (CUL7) XP_011513321.1:p.Val1239GlufsTer11
XM_011515020.1:c.3620_3621del (CUL7) XP_011513322.1:p.Val1207GlufsTer11
XM_011515021.1:c.1325_1326del (CUL7) XP_011513323.1:p.Val442GlufsTer11
XM_005249503.3:c.3620_3621del (CUL7) XP_005249560.1:p.Val1207GlufsTer11
XM_006715285.2:c.3560_3561del (CUL7) XP_006715348.1:p.Val1187GlufsTer11
XM_011515019.2:c.3716_3717del (CUL7) XP_011513321.1:p.Val1239GlufsTer11
XM_011515020.2:c.3620_3621del (CUL7) XP_011513322.1:p.Val1207GlufsTer11
XM_017011533.1:c.3743_3744del (CUL7) XP_016867022.1:p.Val1248GlufsTer11
XM_017011534.1:c.3743_3744del (CUL7) XP_016867023.1:p.Val1248GlufsTer11
XM_017011535.1:c.3647_3648del (CUL7) XP_016867024.1:p.Val1216GlufsTer11
XM_017011536.2:c.3587_3588del (CUL7) XP_016867025.1:p.Val1196GlufsTer11
XM_017011537.2:c.3560_3561del (CUL7) XP_016867026.1:p.Val1187GlufsTer11
XM_017011538.2:c.3491_3492del (CUL7) XP_016867027.1:p.Val1164GlufsTer11
XM_017011539.2:c.3464_3465del (CUL7) XP_016867028.1:p.Val1155GlufsTer11
NM_001168370.2:c.3560_3561del (CUL7) NP_001161842.2:p.Val1187GlufsTer11
NM_001374872.1:c.3560_3561del (CUL7) NP_001361801.1:p.Val1187GlufsTer11
NM_001374873.1:c.3464_3465del (CUL7) NP_001361802.1:p.Val1155GlufsTer11
NM_001374874.1:c.3461_3462del (CUL7) NP_001361803.1:p.Val1154GlufsTer11
NM_014780.5:c.3464_3465del (CUL7) MANE Select NP_055595.2:p.Val1155GlufsTer11