Canonical Allele Identifier: CA351130799

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224557750T>C , CM000664.2:g.224557750T>C	GRCh38
NC_000002.11:g.225422467T>C , CM000664.1:g.225422467T>C	GRCh37
NC_000002.10:g.225130711T>C	NCBI36
NG_032169.1:g.32648A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003590.5:c.173A>G MANE Select	NP_003581.1:p.Tyr58Cys
ENST00000264414.9:c.173A>G MANE Select	ENSP00000264414.4:p.Tyr58Cys
NM_001257197.1:c.67-22109A>G	NP_001244126.1:n.67-22109A>G
NM_001257197.2:c.67-22109A>G	NP_001244126.1:n.67-22109A>G
NM_001257198.1:c.191A>G	NP_001244127.1:p.Tyr64Cys
NM_001257198.2:c.191A>G	NP_001244127.1:p.Tyr64Cys
NM_003590.4:c.173A>G	NP_003581.1:p.Tyr58Cys
ENST00000264414.8:c.173A>G	ENSP00000264414.4:p.Tyr58Cys
ENST00000344951.8:c.67-22109A>G	ENSP00000343601.4:n.67-22109A>G
ENST00000409096.5:c.101A>G	ENSP00000387200.1:p.Tyr34Cys
ENST00000409777.5:c.101A>G	ENSP00000386525.1:p.Tyr34Cys
ENST00000432260.2:c.71A>G	ENSP00000484410.1:p.Tyr24Cys
ENST00000436172.1:c.234A>G
ENST00000546102.1:n.336A>G
XM_006712800.2:c.140A>G	XP_006712863.2:p.Tyr47Cys
XM_011511994.1:c.140A>G	XP_011510296.1:p.Tyr47Cys
XM_011511994.3:c.140A>G	XP_011510296.1:p.Tyr47Cys
XM_011511995.1:c.131A>G	XP_011510297.1:p.Tyr44Cys
XM_011511996.1:c.-146A>G	XP_011510298.1:n.-146A>G
XM_011511996.2:c.-146A>G	XP_011510298.1:n.-146A>G