Canonical Allele Identifier: CA10626891

Gene: CUL7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43037631T>C , CM000668.2:g.43037631T>C	GRCh38
NC_000006.11:g.43005369T>C , CM000668.1:g.43005369T>C	GRCh37
NC_000006.10:g.43113347T>C	NCBI36
NG_016205.1:g.21315A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014780.5:c.*57A>G MANE Select	NP_055595.2:n.*57A>G
ENST00000265348.9:c.*57A>G MANE Select	ENSP00000265348.4:n.*57A>G
NM_001168370.1:c.*57A>G	NP_001161842.1:n.*57A>G
NM_001168370.2:c.*57A>G	NP_001161842.2:n.*57A>G
NM_001374872.1:c.*57A>G	NP_001361801.1:n.*57A>G
NM_001374873.1:c.*57A>G	NP_001361802.1:n.*57A>G
NM_001374874.1:c.*57A>G	NP_001361803.1:n.*57A>G
NM_014780.4:c.*57A>G	NP_055595.2:n.*57A>G
ENST00000265348.7:c.*57A>G	ENSP00000265348.3:n.*57A>G
ENST00000535468.1:c.*57A>G	ENSP00000438788.1:n.*57A>G
ENST00000685042.1:c.*1810A>G	ENSP00000509871.1:n.*1810A>G
ENST00000689256.1:n.5731A>G
ENST00000690231.1:c.*57A>G	ENSP00000508461.1:n.*57A>G
ENST00000692002.1:c.1179A>G	ENSP00000508567.1:n.1179A>G
XM_005249503.1:c.*57A>G	XP_005249560.1:n.*57A>G
XM_005249503.3:c.*57A>G	XP_005249560.1:n.*57A>G
XM_006715285.1:c.*57A>G	XP_006715348.1:n.*57A>G
XM_006715285.2:c.*57A>G	XP_006715348.1:n.*57A>G
XM_011515019.1:c.*57A>G	XP_011513321.1:n.*57A>G
XM_011515019.2:c.*57A>G	XP_011513321.1:n.*57A>G
XM_011515020.1:c.*57A>G	XP_011513322.1:n.*57A>G
XM_011515020.2:c.*57A>G	XP_011513322.1:n.*57A>G
XM_011515021.1:c.*57A>G	XP_011513323.1:n.*57A>G
XM_017011533.1:c.*57A>G	XP_016867022.1:n.*57A>G
XM_017011534.1:c.*57A>G	XP_016867023.1:n.*57A>G
XM_017011535.1:c.*57A>G	XP_016867024.1:n.*57A>G
XM_017011536.2:c.*57A>G	XP_016867025.1:n.*57A>G
XM_017011537.2:c.*57A>G	XP_016867026.1:n.*57A>G
XM_017011538.2:c.*57A>G	XP_016867027.1:n.*57A>G
XM_017011539.2:c.*57A>G	XP_016867028.1:n.*57A>G