Canonical Allele Identifier: CA350827720

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368523A>G (hg19) ; chr2:g.224503806A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503806A>G , CM000664.2:g.224503806A>G	GRCh38
NC_000002.11:g.225368523A>G , CM000664.1:g.225368523A>G	GRCh37
NC_000002.10:g.225076767A>G	NCBI36
NG_032169.1:g.86592T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1223T>C MANE Select	ENSP00000264414.4:p.Val408Ala
ENST00000264414.8:c.1223T>C	ENSP00000264414.4:p.Val408Ala
ENST00000344951.8:c.1025T>C	ENSP00000343601.4:p.Val342Ala
ENST00000409096.5:c.1151T>C	ENSP00000387200.1:p.Val384Ala
ENST00000409777.5:c.1151T>C	ENSP00000386525.1:p.Val384Ala
ENST00000481135.1:n.519T>C
ENST00000617432.4:c.-54T>C	ENSP00000477851.1:n.-54T>C
NM_001257197.1:c.1025T>C	NP_001244126.1:p.Val342Ala
NM_001257198.1:c.1241T>C	NP_001244127.1:p.Val414Ala
NM_003590.4:c.1223T>C	NP_003581.1:p.Val408Ala
XM_006712800.2:c.1190T>C	XP_006712863.2:p.Val397Ala
XM_011511994.1:c.1076T>C	XP_011510296.1:p.Val359Ala
XM_011511995.1:c.1181T>C	XP_011510297.1:p.Val394Ala
XM_011511996.1:c.1031T>C	XP_011510298.1:p.Val344Ala
XM_011511997.1:c.923T>C	XP_011510299.1:p.Val308Ala
XM_011511994.3:c.1076T>C	XP_011510296.1:p.Val359Ala
XM_011511996.2:c.1031T>C	XP_011510298.1:p.Val344Ala
NM_003590.5:c.1223T>C MANE Select	NP_003581.1:p.Val408Ala
NM_001257198.2:c.1241T>C	NP_001244127.1:p.Val414Ala
NM_001257197.2:c.1025T>C	NP_001244126.1:p.Val342Ala