Canonical Allele Identifier: CA1624354978

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043155_43043157delinsCCA , CM000668.2:g.43043155_43043157delinsCCA	GRCh38
NC_000006.11:g.43010893_43010895delinsCCA , CM000668.1:g.43010893_43010895delinsCCA	GRCh37
NC_000006.10:g.43118871_43118873delinsCCA	NCBI36
NG_016205.1:g.15789_15791delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1450_1452delinsTGG (CUL7)
ENST00000674112.2:c.3379_3381delinsTGG (CUL7)	ENSP00000501166.2:p.Trp1127=
ENST00000685042.1:c.*35_*37delinsTGG (CUL7)	ENSP00000509871.1:n.*35_*37delinsTGG
ENST00000686442.1:n.3940_3942delinsTGG (CUL7)
ENST00000687225.1:c.*1676_*1678delinsTGG (CUL7)	ENSP00000509364.1:n.*1676_*1678delinsTGG
ENST00000688302.1:n.3662_3664delinsTGG (CUL7)
ENST00000689256.1:n.3956_3958delinsTGG (CUL7)
ENST00000690231.1:c.3379_3381delinsTGG (CUL7)	ENSP00000508461.1:p.Trp1127=
ENST00000265348.9:c.3379_3381delinsTGG (CUL7) MANE Select	ENSP00000265348.4:p.Trp1127=
ENST00000673725.1:c.1328_1330delinsTGG (CUL7)
ENST00000673753.1:n.4218_4220delinsTGG (CUL7)
ENST00000674100.1:c.3475_3477delinsTGG (CUL7)	ENSP00000501292.1:p.Trp1159=
ENST00000674112.1:c.1871_1873delinsTGG (CUL7)
ENST00000674134.1:c.3475_3477delinsTGG (CUL7)	ENSP00000501068.1:p.Trp1159=
ENST00000265348.7:c.3379_3381delinsTGG (CUL7)	ENSP00000265348.3:p.Trp1127=
ENST00000467906.5:c.-906_-904delinsCCA (KLC4)	ENSP00000418759.1:n.-906_-904delinsCCA
ENST00000535468.1:c.3631_3633delinsTGG (CUL7)	ENSP00000438788.1:p.Trp1211=
NM_001168370.1:c.3631_3633delinsTGG (CUL7)	NP_001161842.1:p.Trp1211=
NM_014780.4:c.3379_3381delinsTGG (CUL7)	NP_055595.2:p.Trp1127=
XM_005249503.1:c.3535_3537delinsTGG (CUL7)	XP_005249560.1:p.Trp1179=
XM_006715285.1:c.3475_3477delinsTGG (CUL7)	XP_006715348.1:p.Trp1159=
XM_011515019.1:c.3631_3633delinsTGG (CUL7)	XP_011513321.1:p.Trp1211=
XM_011515020.1:c.3535_3537delinsTGG (CUL7)	XP_011513322.1:p.Trp1179=
XM_011515021.1:c.1240_1242delinsTGG (CUL7)	XP_011513323.1:p.Trp414=
XM_005249503.3:c.3535_3537delinsTGG (CUL7)	XP_005249560.1:p.Trp1179=
XM_006715285.2:c.3475_3477delinsTGG (CUL7)	XP_006715348.1:p.Trp1159=
XM_011515019.2:c.3631_3633delinsTGG (CUL7)	XP_011513321.1:p.Trp1211=
XM_011515020.2:c.3535_3537delinsTGG (CUL7)	XP_011513322.1:p.Trp1179=
XM_017011533.1:c.3658_3660delinsTGG (CUL7)	XP_016867022.1:p.Trp1220=
XM_017011534.1:c.3658_3660delinsTGG (CUL7)	XP_016867023.1:p.Trp1220=
XM_017011535.1:c.3562_3564delinsTGG (CUL7)	XP_016867024.1:p.Trp1188=
XM_017011536.2:c.3502_3504delinsTGG (CUL7)	XP_016867025.1:p.Trp1168=
XM_017011537.2:c.3475_3477delinsTGG (CUL7)	XP_016867026.1:p.Trp1159=
XM_017011538.2:c.3406_3408delinsTGG (CUL7)	XP_016867027.1:p.Trp1136=
XM_017011539.2:c.3379_3381delinsTGG (CUL7)	XP_016867028.1:p.Trp1127=
NM_001168370.2:c.3475_3477delinsTGG (CUL7)	NP_001161842.2:p.Trp1159=
NM_001374872.1:c.3475_3477delinsTGG (CUL7)	NP_001361801.1:p.Trp1159=
NM_001374873.1:c.3379_3381delinsTGG (CUL7)	NP_001361802.1:p.Trp1127=
NM_001374874.1:c.3376_3378delinsTGG (CUL7)	NP_001361803.1:p.Trp1126=
NM_014780.5:c.3379_3381delinsTGG (CUL7) MANE Select	NP_055595.2:p.Trp1127=