Canonical Allele Identifier: CA913110551

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43010706_43010707insTT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43042969_43042970insTT , CM000668.2:g.43042969_43042970insTT	GRCh38
NC_000006.11:g.43010707_43010708insTT , CM000668.1:g.43010707_43010708insTT	GRCh37
NC_000006.10:g.43118685_43118686insTT	NCBI36
NG_016205.1:g.15977_15978insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1549_1550insAA (CUL7)
ENST00000674112.2:c.3478_3479insAA (CUL7)	ENSP00000501166.2:p.Thr1160LysfsTer?
ENST00000685042.1:c.*134_*135insAA (CUL7)	ENSP00000509871.1:n.*134_*135insAA
ENST00000686442.1:n.4039_4040insAA (CUL7)
ENST00000687225.1:c.*1775_*1776insAA (CUL7)	ENSP00000509364.1:n.*1775_*1776insAA
ENST00000688302.1:n.3761_3762insAA (CUL7)
ENST00000689256.1:n.4055_4056insAA (CUL7)
ENST00000690231.1:c.3478_3479insAA (CUL7)	ENSP00000508461.1:p.Thr1160LysfsTer?
ENST00000265348.9:c.3478_3479insAA (CUL7) MANE Select	ENSP00000265348.4:p.Thr1160LysfsTer?
ENST00000673725.1:c.1412-63_1412-62insAA (CUL7)
ENST00000673753.1:n.4317_4318insAA (CUL7)
ENST00000674100.1:c.3574_3575insAA (CUL7)	ENSP00000501292.1:p.Thr1192LysfsTer?
ENST00000674112.1:c.1970_1971insAA (CUL7)
ENST00000674134.1:c.3574_3575insAA (CUL7)	ENSP00000501068.1:p.Thr1192LysfsTer?
ENST00000265348.7:c.3478_3479insAA (CUL7)	ENSP00000265348.3:p.Thr1160LysfsTer?
ENST00000467906.5:c.-1003-89_-1003-88insTT (KLC4)	ENSP00000418759.1:n.-1003-89_-1003-88insTT
ENST00000535468.1:c.3730_3731insAA (CUL7)	ENSP00000438788.1:p.Thr1244LysfsTer?
NM_001168370.1:c.3730_3731insAA (CUL7)	NP_001161842.1:p.Thr1244LysfsTer?
NM_014780.4:c.3478_3479insAA (CUL7)	NP_055595.2:p.Thr1160LysfsTer?
XM_005249503.1:c.3634_3635insAA (CUL7)	XP_005249560.1:p.Thr1212LysfsTer?
XM_006715285.1:c.3574_3575insAA (CUL7)	XP_006715348.1:p.Thr1192LysfsTer?
XM_011515019.1:c.3730_3731insAA (CUL7)	XP_011513321.1:p.Thr1244LysfsTer?
XM_011515020.1:c.3634_3635insAA (CUL7)	XP_011513322.1:p.Thr1212LysfsTer?
XM_011515021.1:c.1339_1340insAA (CUL7)	XP_011513323.1:p.Thr447LysfsTer?
XM_005249503.3:c.3634_3635insAA (CUL7)	XP_005249560.1:p.Thr1212LysfsTer?
XM_006715285.2:c.3574_3575insAA (CUL7)	XP_006715348.1:p.Thr1192LysfsTer?
XM_011515019.2:c.3730_3731insAA (CUL7)	XP_011513321.1:p.Thr1244LysfsTer?
XM_011515020.2:c.3634_3635insAA (CUL7)	XP_011513322.1:p.Thr1212LysfsTer?
XM_017011533.1:c.3757_3758insAA (CUL7)	XP_016867022.1:p.Thr1253LysfsTer?
XM_017011534.1:c.3757_3758insAA (CUL7)	XP_016867023.1:p.Thr1253LysfsTer?
XM_017011535.1:c.3661_3662insAA (CUL7)	XP_016867024.1:p.Thr1221LysfsTer?
XM_017011536.2:c.3601_3602insAA (CUL7)	XP_016867025.1:p.Thr1201LysfsTer?
XM_017011537.2:c.3574_3575insAA (CUL7)	XP_016867026.1:p.Thr1192LysfsTer?
XM_017011538.2:c.3505_3506insAA (CUL7)	XP_016867027.1:p.Thr1169LysfsTer?
XM_017011539.2:c.3478_3479insAA (CUL7)	XP_016867028.1:p.Thr1160LysfsTer?
NM_001168370.2:c.3574_3575insAA (CUL7)	NP_001161842.2:p.Thr1192LysfsTer?
NM_001374872.1:c.3574_3575insAA (CUL7)	NP_001361801.1:p.Thr1192LysfsTer?
NM_001374873.1:c.3478_3479insAA (CUL7)	NP_001361802.1:p.Thr1160LysfsTer?
NM_001374874.1:c.3475_3476insAA (CUL7)	NP_001361803.1:p.Thr1159LysfsTer?
NM_014780.5:c.3478_3479insAA (CUL7) MANE Select	NP_055595.2:p.Thr1160LysfsTer?