Canonical Allele Identifier: CA364218263

Gene: CUL7 KLC4

Linked Data

• dbSNP Id: rs2150328364
• MyVariant Identifiers: chr6:g.43015917G>T (hg19) ; chr6:g.43048179G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43048179G>T , CM000668.2:g.43048179G>T	GRCh38
NC_000006.11:g.43015917G>T , CM000668.1:g.43015917G>T	GRCh37
NC_000006.10:g.43123895G>T	NCBI36
NG_016205.1:g.10767C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.2138C>A (CUL7)	ENSP00000501166.2:p.Ala713Asp
ENST00000685042.1:c.2138C>A (CUL7)	ENSP00000509871.1:p.Ala713Asp
ENST00000686442.1:n.2421C>A (CUL7)
ENST00000687225.1:c.2234C>A (CUL7)	ENSP00000509364.1:p.Ala745Asp
ENST00000688302.1:n.2421C>A (CUL7)
ENST00000689256.1:n.2437C>A (CUL7)
ENST00000690231.1:c.2138C>A (CUL7)	ENSP00000508461.1:p.Ala713Asp
ENST00000265348.9:c.2138C>A (CUL7) MANE Select	ENSP00000265348.4:p.Ala713Asp
ENST00000673725.1:c.87C>A (CUL7)
ENST00000673753.1:n.2472C>A (CUL7)
ENST00000674100.1:c.2234C>A (CUL7)	ENSP00000501292.1:p.Ala745Asp
ENST00000674112.1:c.630C>A (CUL7)
ENST00000674134.1:c.2234C>A (CUL7)	ENSP00000501068.1:p.Ala745Asp
ENST00000265348.7:c.2138C>A (CUL7)	ENSP00000265348.3:p.Ala713Asp
ENST00000467906.5:c.-553+4671G>T (KLC4)	ENSP00000418759.1:n.-553+4671G>T
ENST00000535468.1:c.2390C>A (CUL7)	ENSP00000438788.1:p.Ala797Asp
NM_001168370.1:c.2390C>A (CUL7)	NP_001161842.1:p.Ala797Asp
NM_014780.4:c.2138C>A (CUL7)	NP_055595.2:p.Ala713Asp
XM_005249503.1:c.2294C>A (CUL7)	XP_005249560.1:p.Ala765Asp
XM_006715285.1:c.2234C>A (CUL7)	XP_006715348.1:p.Ala745Asp
XM_011515019.1:c.2390C>A (CUL7)	XP_011513321.1:p.Ala797Asp
XM_011515020.1:c.2294C>A (CUL7)	XP_011513322.1:p.Ala765Asp
XM_011515021.1:c.-45C>A (CUL7)	XP_011513323.1:n.-45C>A
XM_005249503.3:c.2294C>A (CUL7)	XP_005249560.1:p.Ala765Asp
XM_006715285.2:c.2234C>A (CUL7)	XP_006715348.1:p.Ala745Asp
XM_011515019.2:c.2390C>A (CUL7)	XP_011513321.1:p.Ala797Asp
XM_011515020.2:c.2294C>A (CUL7)	XP_011513322.1:p.Ala765Asp
XM_017011533.1:c.2417C>A (CUL7)	XP_016867022.1:p.Ala806Asp
XM_017011534.1:c.2417C>A (CUL7)	XP_016867023.1:p.Ala806Asp
XM_017011535.1:c.2321C>A (CUL7)	XP_016867024.1:p.Ala774Asp
XM_017011536.2:c.2261C>A (CUL7)	XP_016867025.1:p.Ala754Asp
XM_017011537.2:c.2234C>A (CUL7)	XP_016867026.1:p.Ala745Asp
XM_017011538.2:c.2165C>A (CUL7)	XP_016867027.1:p.Ala722Asp
XM_017011539.2:c.2138C>A (CUL7)	XP_016867028.1:p.Ala713Asp
XM_017011540.1:c.2417C>A (CUL7)	XP_016867029.1:p.Ala806Asp
NM_001168370.2:c.2234C>A (CUL7)	NP_001161842.2:p.Ala745Asp
NM_001374872.1:c.2234C>A (CUL7)	NP_001361801.1:p.Ala745Asp
NM_001374873.1:c.2138C>A (CUL7)	NP_001361802.1:p.Ala713Asp
NM_001374874.1:c.2138C>A (CUL7)	NP_001361803.1:p.Ala713Asp
NM_014780.5:c.2138C>A (CUL7) MANE Select	NP_055595.2:p.Ala713Asp