Canonical Allele Identifier: CA1624357440

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43048625_43048626delinsGA , CM000668.2:g.43048625_43048626delinsGA GRCh38
NC_000006.11:g.43016363_43016364delinsGA , CM000668.1:g.43016363_43016364delinsGA GRCh37
NC_000006.10:g.43124341_43124342delinsGA NCBI36
NG_016205.1:g.10320_10321delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000674112.2:c.1826-57_1826-56delinsTC (CUL7) ENSP00000501166.2:n.1826-57_1826-56delinsTC
ENST00000685042.1:c.1826-57_1826-56delinsTC (CUL7) ENSP00000509871.1:n.1826-57_1826-56delinsTC
ENST00000686442.1:n.2109-57_2109-56delinsTC (CUL7)
ENST00000687225.1:c.1922-57_1922-56delinsTC (CUL7) ENSP00000509364.1:n.1922-57_1922-56delinsTC
ENST00000688302.1:n.2109-57_2109-56delinsTC (CUL7)
ENST00000689256.1:n.2125-57_2125-56delinsTC (CUL7)
ENST00000690231.1:c.1826-57_1826-56delinsTC (CUL7) ENSP00000508461.1:n.1826-57_1826-56delinsTC
ENST00000265348.9:c.1826-57_1826-56delinsTC (CUL7) MANE Select ENSP00000265348.4:n.1826-57_1826-56delinsTC
ENST00000673753.1:n.2160-57_2160-56delinsTC (CUL7)
ENST00000674100.1:c.1922-57_1922-56delinsTC (CUL7) ENSP00000501292.1:n.1922-57_1922-56delinsTC
ENST00000674112.1:c.318-57_318-56delinsTC (CUL7)
ENST00000674134.1:c.1922-57_1922-56delinsTC (CUL7) ENSP00000501068.1:n.1922-57_1922-56delinsTC
ENST00000265348.7:c.1826-57_1826-56delinsTC (CUL7) ENSP00000265348.3:n.1826-57_1826-56delinsTC
ENST00000467906.5:c.-553+5117_-553+5118delinsGA (KLC4) ENSP00000418759.1:n.-553+5117_-553+5118delinsGA
ENST00000535468.1:c.2078-57_2078-56delinsTC (CUL7) ENSP00000438788.1:n.2078-57_2078-56delinsTC
NM_001168370.1:c.2078-57_2078-56delinsTC (CUL7) NP_001161842.1:n.2078-57_2078-56delinsTC
NM_014780.4:c.1826-57_1826-56delinsTC (CUL7) NP_055595.2:n.1826-57_1826-56delinsTC
XM_005249503.1:c.1982-57_1982-56delinsTC (CUL7) XP_005249560.1:n.1982-57_1982-56delinsTC
XM_006715285.1:c.1922-57_1922-56delinsTC (CUL7) XP_006715348.1:n.1922-57_1922-56delinsTC
XM_011515019.1:c.2078-57_2078-56delinsTC (CUL7) XP_011513321.1:n.2078-57_2078-56delinsTC
XM_011515020.1:c.1982-57_1982-56delinsTC (CUL7) XP_011513322.1:n.1982-57_1982-56delinsTC
XM_011515021.1:c.-357-57_-357-56delinsTC (CUL7) XP_011513323.1:n.-357-57_-357-56delinsTC
XM_005249503.3:c.1982-57_1982-56delinsTC (CUL7) XP_005249560.1:n.1982-57_1982-56delinsTC
XM_006715285.2:c.1922-57_1922-56delinsTC (CUL7) XP_006715348.1:n.1922-57_1922-56delinsTC
XM_011515019.2:c.2078-57_2078-56delinsTC (CUL7) XP_011513321.1:n.2078-57_2078-56delinsTC
XM_011515020.2:c.1982-57_1982-56delinsTC (CUL7) XP_011513322.1:n.1982-57_1982-56delinsTC
XM_017011533.1:c.2105-57_2105-56delinsTC (CUL7) XP_016867022.1:n.2105-57_2105-56delinsTC
XM_017011534.1:c.2105-57_2105-56delinsTC (CUL7) XP_016867023.1:n.2105-57_2105-56delinsTC
XM_017011535.1:c.2009-57_2009-56delinsTC (CUL7) XP_016867024.1:n.2009-57_2009-56delinsTC
XM_017011536.2:c.1949-57_1949-56delinsTC (CUL7) XP_016867025.1:n.1949-57_1949-56delinsTC
XM_017011537.2:c.1922-57_1922-56delinsTC (CUL7) XP_016867026.1:n.1922-57_1922-56delinsTC
XM_017011538.2:c.1853-57_1853-56delinsTC (CUL7) XP_016867027.1:n.1853-57_1853-56delinsTC
XM_017011539.2:c.1826-57_1826-56delinsTC (CUL7) XP_016867028.1:n.1826-57_1826-56delinsTC
XM_017011540.1:c.2105-57_2105-56delinsTC (CUL7) XP_016867029.1:n.2105-57_2105-56delinsTC
NM_001168370.2:c.1922-57_1922-56delinsTC (CUL7) NP_001161842.2:n.1922-57_1922-56delinsTC
NM_001374872.1:c.1922-57_1922-56delinsTC (CUL7) NP_001361801.1:n.1922-57_1922-56delinsTC
NM_001374873.1:c.1826-57_1826-56delinsTC (CUL7) NP_001361802.1:n.1826-57_1826-56delinsTC
NM_001374874.1:c.1826-57_1826-56delinsTC (CUL7) NP_001361803.1:n.1826-57_1826-56delinsTC
NM_014780.5:c.1826-57_1826-56delinsTC (CUL7) MANE Select NP_055595.2:n.1826-57_1826-56delinsTC