Canonical Allele Identifier: CA66534321

Gene: CUL3

Linked Data

• dbSNP Id: rs751228695
• gnomAD v3: 2-224503669-T-C
• gnomAD v4: 2-224503669-T-C
• MyVariant Identifiers: chr2:g.225368386T>C (hg19) ; chr2:g.224503669T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503669T>C , CM000664.2:g.224503669T>C	GRCh38
NC_000002.11:g.225368386T>C , CM000664.1:g.225368386T>C	GRCh37
NC_000002.10:g.225076630T>C	NCBI36
NG_032169.1:g.86729A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1360A>G MANE Select	ENSP00000264414.4:p.Met454Val
ENST00000264414.8:c.1360A>G	ENSP00000264414.4:p.Met454Val
ENST00000344951.8:c.1162A>G	ENSP00000343601.4:p.Met388Val
ENST00000409096.5:c.1288A>G	ENSP00000387200.1:p.Met430Val
ENST00000409777.5:c.1288A>G	ENSP00000386525.1:p.Met430Val
ENST00000481135.1:n.656A>G
ENST00000617432.4:c.82A>G	ENSP00000477851.1:p.Met28Val
NM_001257197.1:c.1162A>G	NP_001244126.1:p.Met388Val
NM_001257198.1:c.1378A>G	NP_001244127.1:p.Met460Val
NM_003590.4:c.1360A>G	NP_003581.1:p.Met454Val
XM_006712800.2:c.1327A>G	XP_006712863.2:p.Met443Val
XM_011511994.1:c.1213A>G	XP_011510296.1:p.Met405Val
XM_011511995.1:c.1318A>G	XP_011510297.1:p.Met440Val
XM_011511996.1:c.1168A>G	XP_011510298.1:p.Met390Val
XM_011511997.1:c.1060A>G	XP_011510299.1:p.Met354Val
XM_011511994.3:c.1213A>G	XP_011510296.1:p.Met405Val
XM_011511996.2:c.1168A>G	XP_011510298.1:p.Met390Val
NM_003590.5:c.1360A>G MANE Select	NP_003581.1:p.Met454Val
NM_001257198.2:c.1378A>G	NP_001244127.1:p.Met460Val
NM_001257197.2:c.1162A>G	NP_001244126.1:p.Met388Val