Canonical Allele Identifier: CA350827428

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368452A>G (hg19) ; chr2:g.224503735A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503735A>G , CM000664.2:g.224503735A>G	GRCh38
NC_000002.11:g.225368452A>G , CM000664.1:g.225368452A>G	GRCh37
NC_000002.10:g.225076696A>G	NCBI36
NG_032169.1:g.86663T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1294T>C MANE Select	ENSP00000264414.4:p.Tyr432His
ENST00000264414.8:c.1294T>C	ENSP00000264414.4:p.Tyr432His
ENST00000344951.8:c.1096T>C	ENSP00000343601.4:p.Tyr366His
ENST00000409096.5:c.1222T>C	ENSP00000387200.1:p.Tyr408His
ENST00000409777.5:c.1222T>C	ENSP00000386525.1:p.Tyr408His
ENST00000481135.1:n.590T>C
ENST00000617432.4:c.18T>C	ENSP00000477851.1:p.Ile6=
NM_001257197.1:c.1096T>C	NP_001244126.1:p.Tyr366His
NM_001257198.1:c.1312T>C	NP_001244127.1:p.Tyr438His
NM_003590.4:c.1294T>C	NP_003581.1:p.Tyr432His
XM_006712800.2:c.1261T>C	XP_006712863.2:p.Tyr421His
XM_011511994.1:c.1147T>C	XP_011510296.1:p.Tyr383His
XM_011511995.1:c.1252T>C	XP_011510297.1:p.Tyr418His
XM_011511996.1:c.1102T>C	XP_011510298.1:p.Tyr368His
XM_011511997.1:c.994T>C	XP_011510299.1:p.Tyr332His
XM_011511994.3:c.1147T>C	XP_011510296.1:p.Tyr383His
XM_011511996.2:c.1102T>C	XP_011510298.1:p.Tyr368His
NM_003590.5:c.1294T>C MANE Select	NP_003581.1:p.Tyr432His
NM_001257198.2:c.1312T>C	NP_001244127.1:p.Tyr438His
NM_001257197.2:c.1096T>C	NP_001244126.1:p.Tyr366His