Canonical Allele Identifier: CA1624357241

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43048185_43048187delinsCAG , CM000668.2:g.43048185_43048187delinsCAG	GRCh38
NC_000006.11:g.43015923_43015925delinsCAG , CM000668.1:g.43015923_43015925delinsCAG	GRCh37
NC_000006.10:g.43123901_43123903delinsCAG	NCBI36
NG_016205.1:g.10759_10761delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.2130_2132delinsCTG (CUL7)	ENSP00000501166.2:p.Ala710=
ENST00000685042.1:c.2130_2132delinsCTG (CUL7)	ENSP00000509871.1:p.Ala710=
ENST00000686442.1:n.2413_2415delinsCTG (CUL7)
ENST00000687225.1:c.2226_2228delinsCTG (CUL7)	ENSP00000509364.1:p.Ala742=
ENST00000688302.1:n.2413_2415delinsCTG (CUL7)
ENST00000689256.1:n.2429_2431delinsCTG (CUL7)
ENST00000690231.1:c.2130_2132delinsCTG (CUL7)	ENSP00000508461.1:p.Ala710=
ENST00000265348.9:c.2130_2132delinsCTG (CUL7) MANE Select	ENSP00000265348.4:p.Ala710=
ENST00000673725.1:c.79_81delinsCTG (CUL7)
ENST00000673753.1:n.2464_2466delinsCTG (CUL7)
ENST00000674100.1:c.2226_2228delinsCTG (CUL7)	ENSP00000501292.1:p.Ala742=
ENST00000674112.1:c.622_624delinsCTG (CUL7)
ENST00000674134.1:c.2226_2228delinsCTG (CUL7)	ENSP00000501068.1:p.Ala742=
ENST00000265348.7:c.2130_2132delinsCTG (CUL7)	ENSP00000265348.3:p.Ala710=
ENST00000467906.5:c.-553+4677_-553+4679delinsCAG (KLC4)	ENSP00000418759.1:n.-553+4677_-553+4679delinsCAG
ENST00000535468.1:c.2382_2384delinsCTG (CUL7)	ENSP00000438788.1:p.Ala794=
NM_001168370.1:c.2382_2384delinsCTG (CUL7)	NP_001161842.1:p.Ala794=
NM_014780.4:c.2130_2132delinsCTG (CUL7)	NP_055595.2:p.Ala710=
XM_005249503.1:c.2286_2288delinsCTG (CUL7)	XP_005249560.1:p.Ala762=
XM_006715285.1:c.2226_2228delinsCTG (CUL7)	XP_006715348.1:p.Ala742=
XM_011515019.1:c.2382_2384delinsCTG (CUL7)	XP_011513321.1:p.Ala794=
XM_011515020.1:c.2286_2288delinsCTG (CUL7)	XP_011513322.1:p.Ala762=
XM_011515021.1:c.-53_-51delinsCTG (CUL7)	XP_011513323.1:n.-53_-51delinsCTG
XM_005249503.3:c.2286_2288delinsCTG (CUL7)	XP_005249560.1:p.Ala762=
XM_006715285.2:c.2226_2228delinsCTG (CUL7)	XP_006715348.1:p.Ala742=
XM_011515019.2:c.2382_2384delinsCTG (CUL7)	XP_011513321.1:p.Ala794=
XM_011515020.2:c.2286_2288delinsCTG (CUL7)	XP_011513322.1:p.Ala762=
XM_017011533.1:c.2409_2411delinsCTG (CUL7)	XP_016867022.1:p.Ala803=
XM_017011534.1:c.2409_2411delinsCTG (CUL7)	XP_016867023.1:p.Ala803=
XM_017011535.1:c.2313_2315delinsCTG (CUL7)	XP_016867024.1:p.Ala771=
XM_017011536.2:c.2253_2255delinsCTG (CUL7)	XP_016867025.1:p.Ala751=
XM_017011537.2:c.2226_2228delinsCTG (CUL7)	XP_016867026.1:p.Ala742=
XM_017011538.2:c.2157_2159delinsCTG (CUL7)	XP_016867027.1:p.Ala719=
XM_017011539.2:c.2130_2132delinsCTG (CUL7)	XP_016867028.1:p.Ala710=
XM_017011540.1:c.2409_2411delinsCTG (CUL7)	XP_016867029.1:p.Ala803=
NM_001168370.2:c.2226_2228delinsCTG (CUL7)	NP_001161842.2:p.Ala742=
NM_001374872.1:c.2226_2228delinsCTG (CUL7)	NP_001361801.1:p.Ala742=
NM_001374873.1:c.2130_2132delinsCTG (CUL7)	NP_001361802.1:p.Ala710=
NM_001374874.1:c.2130_2132delinsCTG (CUL7)	NP_001361803.1:p.Ala710=
NM_014780.5:c.2130_2132delinsCTG (CUL7) MANE Select	NP_055595.2:p.Ala710=