Canonical Allele Identifier: CA350827518

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368469T>G (hg19) ; chr2:g.224503752T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503752T>G , CM000664.2:g.224503752T>G	GRCh38
NC_000002.11:g.225368469T>G , CM000664.1:g.225368469T>G	GRCh37
NC_000002.10:g.225076713T>G	NCBI36
NG_032169.1:g.86646A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1277A>C MANE Select	ENSP00000264414.4:p.Asp426Ala
ENST00000264414.8:c.1277A>C	ENSP00000264414.4:p.Asp426Ala
ENST00000344951.8:c.1079A>C	ENSP00000343601.4:p.Asp360Ala
ENST00000409096.5:c.1205A>C	ENSP00000387200.1:p.Asp402Ala
ENST00000409777.5:c.1205A>C	ENSP00000386525.1:p.Asp402Ala
ENST00000481135.1:n.573A>C
ENST00000617432.4:c.1A>C	ENSP00000477851.1:p.Met1Leu
NM_001257197.1:c.1079A>C	NP_001244126.1:p.Asp360Ala
NM_001257198.1:c.1295A>C	NP_001244127.1:p.Asp432Ala
NM_003590.4:c.1277A>C	NP_003581.1:p.Asp426Ala
XM_006712800.2:c.1244A>C	XP_006712863.2:p.Asp415Ala
XM_011511994.1:c.1130A>C	XP_011510296.1:p.Asp377Ala
XM_011511995.1:c.1235A>C	XP_011510297.1:p.Asp412Ala
XM_011511996.1:c.1085A>C	XP_011510298.1:p.Asp362Ala
XM_011511997.1:c.977A>C	XP_011510299.1:p.Asp326Ala
XM_011511994.3:c.1130A>C	XP_011510296.1:p.Asp377Ala
XM_011511996.2:c.1085A>C	XP_011510298.1:p.Asp362Ala
NM_003590.5:c.1277A>C MANE Select	NP_003581.1:p.Asp426Ala
NM_001257198.2:c.1295A>C	NP_001244127.1:p.Asp432Ala
NM_001257197.2:c.1079A>C	NP_001244126.1:p.Asp360Ala