Canonical Allele Identifier: CA1624357394

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43048487_43048490delinsCAGG , CM000668.2:g.43048487_43048490delinsCAGG	GRCh38
NC_000006.11:g.43016225_43016228delinsCAGG , CM000668.1:g.43016225_43016228delinsCAGG	GRCh37
NC_000006.10:g.43124203_43124206delinsCAGG	NCBI36
NG_016205.1:g.10456_10459delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.1905_1908delinsCCTG (CUL7)	ENSP00000501166.2:p.Leu635=
ENST00000685042.1:c.1905_1908delinsCCTG (CUL7)	ENSP00000509871.1:p.Leu635=
ENST00000686442.1:n.2188_2191delinsCCTG (CUL7)
ENST00000687225.1:c.2001_2004delinsCCTG (CUL7)	ENSP00000509364.1:p.Leu667=
ENST00000688302.1:n.2188_2191delinsCCTG (CUL7)
ENST00000689256.1:n.2204_2207delinsCCTG (CUL7)
ENST00000690231.1:c.1905_1908delinsCCTG (CUL7)	ENSP00000508461.1:p.Leu635=
ENST00000265348.9:c.1905_1908delinsCCTG (CUL7) MANE Select	ENSP00000265348.4:p.Leu635=
ENST00000673753.1:n.2239_2242delinsCCTG (CUL7)
ENST00000674100.1:c.2001_2004delinsCCTG (CUL7)	ENSP00000501292.1:p.Leu667=
ENST00000674112.1:c.397_400delinsCCTG (CUL7)
ENST00000674134.1:c.2001_2004delinsCCTG (CUL7)	ENSP00000501068.1:p.Leu667=
ENST00000265348.7:c.1905_1908delinsCCTG (CUL7)	ENSP00000265348.3:p.Leu635=
ENST00000467906.5:c.-553+4979_-553+4982delinsCAGG (KLC4)	ENSP00000418759.1:n.-553+4979_-553+4982delinsCAGG
ENST00000535468.1:c.2157_2160delinsCCTG (CUL7)	ENSP00000438788.1:p.Leu719=
NM_001168370.1:c.2157_2160delinsCCTG (CUL7)	NP_001161842.1:p.Leu719=
NM_014780.4:c.1905_1908delinsCCTG (CUL7)	NP_055595.2:p.Leu635=
XM_005249503.1:c.2061_2064delinsCCTG (CUL7)	XP_005249560.1:p.Leu687=
XM_006715285.1:c.2001_2004delinsCCTG (CUL7)	XP_006715348.1:p.Leu667=
XM_011515019.1:c.2157_2160delinsCCTG (CUL7)	XP_011513321.1:p.Leu719=
XM_011515020.1:c.2061_2064delinsCCTG (CUL7)	XP_011513322.1:p.Leu687=
XM_011515021.1:c.-278_-275delinsCCTG (CUL7)	XP_011513323.1:n.-278_-275delinsCCTG
XM_005249503.3:c.2061_2064delinsCCTG (CUL7)	XP_005249560.1:p.Leu687=
XM_006715285.2:c.2001_2004delinsCCTG (CUL7)	XP_006715348.1:p.Leu667=
XM_011515019.2:c.2157_2160delinsCCTG (CUL7)	XP_011513321.1:p.Leu719=
XM_011515020.2:c.2061_2064delinsCCTG (CUL7)	XP_011513322.1:p.Leu687=
XM_017011533.1:c.2184_2187delinsCCTG (CUL7)	XP_016867022.1:p.Leu728=
XM_017011534.1:c.2184_2187delinsCCTG (CUL7)	XP_016867023.1:p.Leu728=
XM_017011535.1:c.2088_2091delinsCCTG (CUL7)	XP_016867024.1:p.Leu696=
XM_017011536.2:c.2028_2031delinsCCTG (CUL7)	XP_016867025.1:p.Leu676=
XM_017011537.2:c.2001_2004delinsCCTG (CUL7)	XP_016867026.1:p.Leu667=
XM_017011538.2:c.1932_1935delinsCCTG (CUL7)	XP_016867027.1:p.Leu644=
XM_017011539.2:c.1905_1908delinsCCTG (CUL7)	XP_016867028.1:p.Leu635=
XM_017011540.1:c.2184_2187delinsCCTG (CUL7)	XP_016867029.1:p.Leu728=
NM_001168370.2:c.2001_2004delinsCCTG (CUL7)	NP_001161842.2:p.Leu667=
NM_001374872.1:c.2001_2004delinsCCTG (CUL7)	NP_001361801.1:p.Leu667=
NM_001374873.1:c.1905_1908delinsCCTG (CUL7)	NP_001361802.1:p.Leu635=
NM_001374874.1:c.1905_1908delinsCCTG (CUL7)	NP_001361803.1:p.Leu635=
NM_014780.5:c.1905_1908delinsCCTG (CUL7) MANE Select	NP_055595.2:p.Leu635=