Canonical Allele Identifier: CA450369573

Gene: CUL7 KLC4

Linked Data

• gnomAD v4: 6-43043089-G-C
• MyVariant Identifiers: chr6:g.43010827G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043089G>C , CM000668.2:g.43043089G>C	GRCh38
NC_000006.11:g.43010827G>C , CM000668.1:g.43010827G>C	GRCh37
NC_000006.10:g.43118805G>C	NCBI36
NG_016205.1:g.15857C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.1518C>G (CUL7)
ENST00000674112.2:c.3447C>G (CUL7)	ENSP00000501166.2:p.Ala1149=
ENST00000685042.1:c.*103C>G (CUL7)	ENSP00000509871.1:n.*103C>G
ENST00000686442.1:n.4008C>G (CUL7)
ENST00000687225.1:c.*1744C>G (CUL7)	ENSP00000509364.1:n.*1744C>G
ENST00000688302.1:n.3730C>G (CUL7)
ENST00000689256.1:n.4024C>G (CUL7)
ENST00000690231.1:c.3447C>G (CUL7)	ENSP00000508461.1:p.Ala1149=
ENST00000265348.9:c.3447C>G (CUL7) MANE Select	ENSP00000265348.4:p.Ala1149=
ENST00000673725.1:c.1396C>G (CUL7)
ENST00000673753.1:n.4286C>G (CUL7)
ENST00000674100.1:c.3543C>G (CUL7)	ENSP00000501292.1:p.Ala1181=
ENST00000674112.1:c.1939C>G (CUL7)
ENST00000674134.1:c.3543C>G (CUL7)	ENSP00000501068.1:p.Ala1181=
ENST00000265348.7:c.3447C>G (CUL7)	ENSP00000265348.3:p.Ala1149=
ENST00000467906.5:c.-972G>C (KLC4)	ENSP00000418759.1:n.-972G>C
ENST00000535468.1:c.3699C>G (CUL7)	ENSP00000438788.1:p.Ala1233=
NM_001168370.1:c.3699C>G (CUL7)	NP_001161842.1:p.Ala1233=
NM_014780.4:c.3447C>G (CUL7)	NP_055595.2:p.Ala1149=
XM_005249503.1:c.3603C>G (CUL7)	XP_005249560.1:p.Ala1201=
XM_006715285.1:c.3543C>G (CUL7)	XP_006715348.1:p.Ala1181=
XM_011515019.1:c.3699C>G (CUL7)	XP_011513321.1:p.Ala1233=
XM_011515020.1:c.3603C>G (CUL7)	XP_011513322.1:p.Ala1201=
XM_011515021.1:c.1308C>G (CUL7)	XP_011513323.1:p.Ala436=
XM_005249503.3:c.3603C>G (CUL7)	XP_005249560.1:p.Ala1201=
XM_006715285.2:c.3543C>G (CUL7)	XP_006715348.1:p.Ala1181=
XM_011515019.2:c.3699C>G (CUL7)	XP_011513321.1:p.Ala1233=
XM_011515020.2:c.3603C>G (CUL7)	XP_011513322.1:p.Ala1201=
XM_017011533.1:c.3726C>G (CUL7)	XP_016867022.1:p.Ala1242=
XM_017011534.1:c.3726C>G (CUL7)	XP_016867023.1:p.Ala1242=
XM_017011535.1:c.3630C>G (CUL7)	XP_016867024.1:p.Ala1210=
XM_017011536.2:c.3570C>G (CUL7)	XP_016867025.1:p.Ala1190=
XM_017011537.2:c.3543C>G (CUL7)	XP_016867026.1:p.Ala1181=
XM_017011538.2:c.3474C>G (CUL7)	XP_016867027.1:p.Ala1158=
XM_017011539.2:c.3447C>G (CUL7)	XP_016867028.1:p.Ala1149=
NM_001168370.2:c.3543C>G (CUL7)	NP_001161842.2:p.Ala1181=
NM_001374872.1:c.3543C>G (CUL7)	NP_001361801.1:p.Ala1181=
NM_001374873.1:c.3447C>G (CUL7)	NP_001361802.1:p.Ala1149=
NM_001374874.1:c.3444C>G (CUL7)	NP_001361803.1:p.Ala1148=
NM_014780.5:c.3447C>G (CUL7) MANE Select	NP_055595.2:p.Ala1149=