Canonical Allele Identifier: CA2678806362

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43043181_43043182del , CM000668.2:g.43043181_43043182del GRCh38
NC_000006.11:g.43010919_43010920del , CM000668.1:g.43010919_43010920del GRCh37
NC_000006.10:g.43118897_43118898del NCBI36
NG_016205.1:g.15765_15766del

Transcript Alleles

HGVS Amino-acid Change
ENST00000478630.2:n.1427-1_1427del (CUL7)
ENST00000674112.2:c.3356-1_3356del (CUL7)
ENST00000685042.1:c.*12-1_*12del (CUL7)
ENST00000686442.1:n.3917-1_3917del (CUL7)
ENST00000687225.1:c.*1653-1_*1653del (CUL7)
ENST00000688302.1:n.3639-1_3639del (CUL7)
ENST00000689256.1:n.3933-1_3933del (CUL7)
ENST00000690231.1:c.3356-1_3356del (CUL7)
ENST00000265348.9:c.3356-1_3356del (CUL7)
ENST00000673725.1:c.1305-1_1305del (CUL7)
ENST00000673753.1:n.4195-1_4195del (CUL7)
ENST00000674100.1:c.3452-1_3452del (CUL7)
ENST00000674112.1:c.1848-1_1848del (CUL7)
ENST00000674134.1:c.3452-1_3452del (CUL7)
ENST00000265348.7:c.3356-1_3356del (CUL7)
ENST00000467906.5:c.-880_-879del (KLC4) ENSP00000418759.1:n.-880_-879del
ENST00000535468.1:c.3608-1_3608del (CUL7)
NM_001168370.1:c.3608-1_3608del (CUL7)
NM_014780.4:c.3356-1_3356del (CUL7)
XM_005249503.1:c.3512-1_3512del (CUL7)
XM_006715285.1:c.3452-1_3452del (CUL7)
XM_011515019.1:c.3608-1_3608del (CUL7)
XM_011515020.1:c.3512-1_3512del (CUL7)
XM_011515021.1:c.1217-1_1217del (CUL7)
XM_005249503.3:c.3512-1_3512del (CUL7)
XM_006715285.2:c.3452-1_3452del (CUL7)
XM_011515019.2:c.3608-1_3608del (CUL7)
XM_011515020.2:c.3512-1_3512del (CUL7)
XM_017011533.1:c.3635-1_3635del (CUL7)
XM_017011534.1:c.3635-1_3635del (CUL7)
XM_017011535.1:c.3539-1_3539del (CUL7)
XM_017011536.2:c.3479-1_3479del (CUL7)
XM_017011537.2:c.3452-1_3452del (CUL7)
XM_017011538.2:c.3383-1_3383del (CUL7)
XM_017011539.2:c.3356-1_3356del (CUL7)
NM_001168370.2:c.3452-1_3452del (CUL7)
NM_001374872.1:c.3452-1_3452del (CUL7)
NM_001374873.1:c.3356-1_3356del (CUL7)
NM_001374874.1:c.3356-4_3356-3del (CUL7) NP_001361803.1:n.3356-4_3356-3del
NM_014780.5:c.3356-1_3356del (CUL7)