Canonical Allele Identifier: CA3813492

Gene: CUL7 KLC4

Linked Data

• dbSNP Id: rs780247413
• ExAC: 6:43010843 G / A
• gnomAD v2: 6-43010843-G-A
• gnomAD v3: 6-43043105-G-A
• gnomAD v4: 6-43043105-G-A
• MyVariant Identifiers: chr6:g.43010843G>A (hg19) ; chr6:g.43043105G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43043105G>A , CM000668.2:g.43043105G>A	GRCh38
NC_000006.11:g.43010843G>A , CM000668.1:g.43010843G>A	GRCh37
NC_000006.10:g.43118821G>A	NCBI36
NG_016205.1:g.15841C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000478630.2:n.1502C>T (CUL7)
ENST00000674112.2:c.3431C>T (CUL7)	ENSP00000501166.2:p.Thr1144Met
ENST00000685042.1:c.*87C>T (CUL7)	ENSP00000509871.1:n.*87C>T
ENST00000686442.1:n.3992C>T (CUL7)
ENST00000687225.1:c.*1728C>T (CUL7)	ENSP00000509364.1:n.*1728C>T
ENST00000688302.1:n.3714C>T (CUL7)
ENST00000689256.1:n.4008C>T (CUL7)
ENST00000690231.1:c.3431C>T (CUL7)	ENSP00000508461.1:p.Thr1144Met
ENST00000265348.9:c.3431C>T (CUL7) MANE Select	ENSP00000265348.4:p.Thr1144Met
ENST00000673725.1:c.1380C>T (CUL7)
ENST00000673753.1:n.4270C>T (CUL7)
ENST00000674100.1:c.3527C>T (CUL7)	ENSP00000501292.1:p.Thr1176Met
ENST00000674112.1:c.1923C>T (CUL7)
ENST00000674134.1:c.3527C>T (CUL7)	ENSP00000501068.1:p.Thr1176Met
ENST00000265348.7:c.3431C>T (CUL7)	ENSP00000265348.3:p.Thr1144Met
ENST00000467906.5:c.-956G>A (KLC4)	ENSP00000418759.1:n.-956G>A
ENST00000535468.1:c.3683C>T (CUL7)	ENSP00000438788.1:p.Thr1228Met
NM_001168370.1:c.3683C>T (CUL7)	NP_001161842.1:p.Thr1228Met
NM_014780.4:c.3431C>T (CUL7)	NP_055595.2:p.Thr1144Met
XM_005249503.1:c.3587C>T (CUL7)	XP_005249560.1:p.Thr1196Met
XM_006715285.1:c.3527C>T (CUL7)	XP_006715348.1:p.Thr1176Met
XM_011515019.1:c.3683C>T (CUL7)	XP_011513321.1:p.Thr1228Met
XM_011515020.1:c.3587C>T (CUL7)	XP_011513322.1:p.Thr1196Met
XM_011515021.1:c.1292C>T (CUL7)	XP_011513323.1:p.Thr431Met
XM_005249503.3:c.3587C>T (CUL7)	XP_005249560.1:p.Thr1196Met
XM_006715285.2:c.3527C>T (CUL7)	XP_006715348.1:p.Thr1176Met
XM_011515019.2:c.3683C>T (CUL7)	XP_011513321.1:p.Thr1228Met
XM_011515020.2:c.3587C>T (CUL7)	XP_011513322.1:p.Thr1196Met
XM_017011533.1:c.3710C>T (CUL7)	XP_016867022.1:p.Thr1237Met
XM_017011534.1:c.3710C>T (CUL7)	XP_016867023.1:p.Thr1237Met
XM_017011535.1:c.3614C>T (CUL7)	XP_016867024.1:p.Thr1205Met
XM_017011536.2:c.3554C>T (CUL7)	XP_016867025.1:p.Thr1185Met
XM_017011537.2:c.3527C>T (CUL7)	XP_016867026.1:p.Thr1176Met
XM_017011538.2:c.3458C>T (CUL7)	XP_016867027.1:p.Thr1153Met
XM_017011539.2:c.3431C>T (CUL7)	XP_016867028.1:p.Thr1144Met
NM_001168370.2:c.3527C>T (CUL7)	NP_001161842.2:p.Thr1176Met
NM_001374872.1:c.3527C>T (CUL7)	NP_001361801.1:p.Thr1176Met
NM_001374873.1:c.3431C>T (CUL7)	NP_001361802.1:p.Thr1144Met
NM_001374874.1:c.3428C>T (CUL7)	NP_001361803.1:p.Thr1143Met
NM_014780.5:c.3431C>T (CUL7) MANE Select	NP_055595.2:p.Thr1144Met