Canonical Allele Identifier: CA350827506

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197169
• MyVariant Identifiers: chr2:g.225368467C>G (hg19) ; chr2:g.224503750C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503750C>G , CM000664.2:g.224503750C>G	GRCh38
NC_000002.11:g.225368467C>G , CM000664.1:g.225368467C>G	GRCh37
NC_000002.10:g.225076711C>G	NCBI36
NG_032169.1:g.86648G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1279G>C MANE Select	ENSP00000264414.4:p.Val427Leu
ENST00000264414.8:c.1279G>C	ENSP00000264414.4:p.Val427Leu
ENST00000344951.8:c.1081G>C	ENSP00000343601.4:p.Val361Leu
ENST00000409096.5:c.1207G>C	ENSP00000387200.1:p.Val403Leu
ENST00000409777.5:c.1207G>C	ENSP00000386525.1:p.Val403Leu
ENST00000481135.1:n.575G>C
ENST00000617432.4:c.3G>C	ENSP00000477851.1:p.Met1Ile
NM_001257197.1:c.1081G>C	NP_001244126.1:p.Val361Leu
NM_001257198.1:c.1297G>C	NP_001244127.1:p.Val433Leu
NM_003590.4:c.1279G>C	NP_003581.1:p.Val427Leu
XM_006712800.2:c.1246G>C	XP_006712863.2:p.Val416Leu
XM_011511994.1:c.1132G>C	XP_011510296.1:p.Val378Leu
XM_011511995.1:c.1237G>C	XP_011510297.1:p.Val413Leu
XM_011511996.1:c.1087G>C	XP_011510298.1:p.Val363Leu
XM_011511997.1:c.979G>C	XP_011510299.1:p.Val327Leu
XM_011511994.3:c.1132G>C	XP_011510296.1:p.Val378Leu
XM_011511996.2:c.1087G>C	XP_011510298.1:p.Val363Leu
NM_003590.5:c.1279G>C MANE Select	NP_003581.1:p.Val427Leu
NM_001257198.2:c.1297G>C	NP_001244127.1:p.Val433Leu
NM_001257197.2:c.1081G>C	NP_001244126.1:p.Val361Leu