Canonical Allele Identifier: CA1624357382

Linked Data

dbSNP Id: rs1764116391

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43048471_43048484del , CM000668.2:g.43048471_43048484del GRCh38
NC_000006.11:g.43016209_43016222del , CM000668.1:g.43016209_43016222del GRCh37
NC_000006.10:g.43124187_43124200del NCBI36
NG_016205.1:g.10464_10477del

Transcript Alleles

HGVS Amino-acid Change
ENST00000674112.2:c.1913_1926del (CUL7) ENSP00000501166.2:p.Leu638GlnfsTer?
ENST00000685042.1:c.1913_1926del (CUL7) ENSP00000509871.1:p.Leu638GlnfsTer?
ENST00000686442.1:n.2196_2209del (CUL7)
ENST00000687225.1:c.2009_2022del (CUL7) ENSP00000509364.1:p.Leu670GlnfsTer?
ENST00000688302.1:n.2196_2209del (CUL7)
ENST00000689256.1:n.2212_2225del (CUL7)
ENST00000690231.1:c.1913_1926del (CUL7) ENSP00000508461.1:p.Leu638GlnfsTer?
ENST00000265348.9:c.1913_1926del (CUL7) MANE Select ENSP00000265348.4:p.Leu638GlnfsTer?
ENST00000673753.1:n.2247_2260del (CUL7)
ENST00000674100.1:c.2009_2022del (CUL7) ENSP00000501292.1:p.Leu670GlnfsTer?
ENST00000674112.1:c.405_418del (CUL7)
ENST00000674134.1:c.2009_2022del (CUL7) ENSP00000501068.1:p.Leu670GlnfsTer?
ENST00000265348.7:c.1913_1926del (CUL7) ENSP00000265348.3:p.Leu638GlnfsTer?
ENST00000467906.5:c.-553+4963_-553+4976del (KLC4) ENSP00000418759.1:n.-553+4963_-553+4976del
ENST00000535468.1:c.2165_2178del (CUL7) ENSP00000438788.1:p.Leu722GlnfsTer?
NM_001168370.1:c.2165_2178del (CUL7) NP_001161842.1:p.Leu722GlnfsTer?
NM_014780.4:c.1913_1926del (CUL7) NP_055595.2:p.Leu638GlnfsTer?
XM_005249503.1:c.2069_2082del (CUL7) XP_005249560.1:p.Leu690GlnfsTer?
XM_006715285.1:c.2009_2022del (CUL7) XP_006715348.1:p.Leu670GlnfsTer?
XM_011515019.1:c.2165_2178del (CUL7) XP_011513321.1:p.Leu722GlnfsTer?
XM_011515020.1:c.2069_2082del (CUL7) XP_011513322.1:p.Leu690GlnfsTer?
XM_011515021.1:c.-270_-257del (CUL7) XP_011513323.1:n.-270_-257del
XM_005249503.3:c.2069_2082del (CUL7) XP_005249560.1:p.Leu690GlnfsTer?
XM_006715285.2:c.2009_2022del (CUL7) XP_006715348.1:p.Leu670GlnfsTer?
XM_011515019.2:c.2165_2178del (CUL7) XP_011513321.1:p.Leu722GlnfsTer?
XM_011515020.2:c.2069_2082del (CUL7) XP_011513322.1:p.Leu690GlnfsTer?
XM_017011533.1:c.2192_2205del (CUL7) XP_016867022.1:p.Leu731GlnfsTer?
XM_017011534.1:c.2192_2205del (CUL7) XP_016867023.1:p.Leu731GlnfsTer?
XM_017011535.1:c.2096_2109del (CUL7) XP_016867024.1:p.Leu699GlnfsTer?
XM_017011536.2:c.2036_2049del (CUL7) XP_016867025.1:p.Leu679GlnfsTer?
XM_017011537.2:c.2009_2022del (CUL7) XP_016867026.1:p.Leu670GlnfsTer?
XM_017011538.2:c.1940_1953del (CUL7) XP_016867027.1:p.Leu647GlnfsTer?
XM_017011539.2:c.1913_1926del (CUL7) XP_016867028.1:p.Leu638GlnfsTer?
XM_017011540.1:c.2192_2205del (CUL7) XP_016867029.1:p.Leu731GlnfsTer?
NM_001168370.2:c.2009_2022del (CUL7) NP_001161842.2:p.Leu670GlnfsTer?
NM_001374872.1:c.2009_2022del (CUL7) NP_001361801.1:p.Leu670GlnfsTer?
NM_001374873.1:c.1913_1926del (CUL7) NP_001361802.1:p.Leu638GlnfsTer?
NM_001374874.1:c.1913_1926del (CUL7) NP_001361803.1:p.Leu638GlnfsTer?
NM_014780.5:c.1913_1926del (CUL7) MANE Select NP_055595.2:p.Leu638GlnfsTer?