Canonical Allele Identifier: CA1624357380

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43048468_43048482delinsTGAGGGCTTGCTCTA , CM000668.2:g.43048468_43048482delinsTGAGGGCTTGCTCTA	GRCh38
NC_000006.11:g.43016206_43016220delinsTGAGGGCTTGCTCTA , CM000668.1:g.43016206_43016220delinsTGAGGGCTTGCTCTA	GRCh37
NC_000006.10:g.43124184_43124198delinsTGAGGGCTTGCTCTA	NCBI36
NG_016205.1:g.10464_10478delinsTAGAGCAAGCCCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7)	ENSP00000501166.2:p.Leu638=
ENST00000685042.1:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7)	ENSP00000509871.1:p.Leu638=
ENST00000686442.1:n.2196_2210delinsTAGAGCAAGCCCTCA (CUL7)
ENST00000687225.1:c.2009_2023delinsTAGAGCAAGCCCTCA (CUL7)	ENSP00000509364.1:p.Leu670=
ENST00000688302.1:n.2196_2210delinsTAGAGCAAGCCCTCA (CUL7)
ENST00000689256.1:n.2212_2226delinsTAGAGCAAGCCCTCA (CUL7)
ENST00000690231.1:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7)	ENSP00000508461.1:p.Leu638=
ENST00000265348.9:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7) MANE Select	ENSP00000265348.4:p.Leu638=
ENST00000673753.1:n.2247_2261delinsTAGAGCAAGCCCTCA (CUL7)
ENST00000674100.1:c.2009_2023delinsTAGAGCAAGCCCTCA (CUL7)	ENSP00000501292.1:p.Leu670=
ENST00000674112.1:c.405_419delinsTAGAGCAAGCCCTCA (CUL7)
ENST00000674134.1:c.2009_2023delinsTAGAGCAAGCCCTCA (CUL7)	ENSP00000501068.1:p.Leu670=
ENST00000265348.7:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7)	ENSP00000265348.3:p.Leu638=
ENST00000467906.5:c.-553+4960_-553+4974delinsTGAGGGCTTGCTCTA (KLC4)	ENSP00000418759.1:n.-553+4960_-553+4974delinsTGAGGGCTTGCTCTA
ENST00000535468.1:c.2165_2179delinsTAGAGCAAGCCCTCA (CUL7)	ENSP00000438788.1:p.Leu722=
NM_001168370.1:c.2165_2179delinsTAGAGCAAGCCCTCA (CUL7)	NP_001161842.1:p.Leu722=
NM_014780.4:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7)	NP_055595.2:p.Leu638=
XM_005249503.1:c.2069_2083delinsTAGAGCAAGCCCTCA (CUL7)	XP_005249560.1:p.Leu690=
XM_006715285.1:c.2009_2023delinsTAGAGCAAGCCCTCA (CUL7)	XP_006715348.1:p.Leu670=
XM_011515019.1:c.2165_2179delinsTAGAGCAAGCCCTCA (CUL7)	XP_011513321.1:p.Leu722=
XM_011515020.1:c.2069_2083delinsTAGAGCAAGCCCTCA (CUL7)	XP_011513322.1:p.Leu690=
XM_011515021.1:c.-270_-256delinsTAGAGCAAGCCCTCA (CUL7)	XP_011513323.1:n.-270_-256delinsTAGAGCAAGCCCTCA
XM_005249503.3:c.2069_2083delinsTAGAGCAAGCCCTCA (CUL7)	XP_005249560.1:p.Leu690=
XM_006715285.2:c.2009_2023delinsTAGAGCAAGCCCTCA (CUL7)	XP_006715348.1:p.Leu670=
XM_011515019.2:c.2165_2179delinsTAGAGCAAGCCCTCA (CUL7)	XP_011513321.1:p.Leu722=
XM_011515020.2:c.2069_2083delinsTAGAGCAAGCCCTCA (CUL7)	XP_011513322.1:p.Leu690=
XM_017011533.1:c.2192_2206delinsTAGAGCAAGCCCTCA (CUL7)	XP_016867022.1:p.Leu731=
XM_017011534.1:c.2192_2206delinsTAGAGCAAGCCCTCA (CUL7)	XP_016867023.1:p.Leu731=
XM_017011535.1:c.2096_2110delinsTAGAGCAAGCCCTCA (CUL7)	XP_016867024.1:p.Leu699=
XM_017011536.2:c.2036_2050delinsTAGAGCAAGCCCTCA (CUL7)	XP_016867025.1:p.Leu679=
XM_017011537.2:c.2009_2023delinsTAGAGCAAGCCCTCA (CUL7)	XP_016867026.1:p.Leu670=
XM_017011538.2:c.1940_1954delinsTAGAGCAAGCCCTCA (CUL7)	XP_016867027.1:p.Leu647=
XM_017011539.2:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7)	XP_016867028.1:p.Leu638=
XM_017011540.1:c.2192_2206delinsTAGAGCAAGCCCTCA (CUL7)	XP_016867029.1:p.Leu731=
NM_001168370.2:c.2009_2023delinsTAGAGCAAGCCCTCA (CUL7)	NP_001161842.2:p.Leu670=
NM_001374872.1:c.2009_2023delinsTAGAGCAAGCCCTCA (CUL7)	NP_001361801.1:p.Leu670=
NM_001374873.1:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7)	NP_001361802.1:p.Leu638=
NM_001374874.1:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7)	NP_001361803.1:p.Leu638=
NM_014780.5:c.1913_1927delinsTAGAGCAAGCCCTCA (CUL7) MANE Select	NP_055595.2:p.Leu638=