Canonical Allele Identifier: CA10614374

Gene: CUL3

Linked Data

• ClinVar Variation Id: 334618
• ClinVar RCV Id: RCV000329801 ; RCV001137209
• dbSNP Id: rs3768897
• gnomAD v2: 2-225338022-G-A
• gnomAD v3: 2-224473305-G-A
• gnomAD v4: 2-224473305-G-A
• MyVariant Identifiers: chr2:g.225338022G>A (hg19) ; chr2:g.224473305G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224473305G>A , CM000664.2:g.224473305G>A	GRCh38
NC_000002.11:g.225338022G>A , CM000664.1:g.225338022G>A	GRCh37
NC_000002.10:g.225046266G>A	NCBI36
NG_032169.1:g.117093C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.*940C>T MANE Select	ENSP00000264414.4:n.*940C>T
ENST00000264414.8:c.*940C>T	ENSP00000264414.4:n.*940C>T
ENST00000344951.8:c.*940C>T	ENSP00000343601.4:n.*940C>T
NM_001257197.1:c.*940C>T	NP_001244126.1:n.*940C>T
NM_001257198.1:c.*940C>T	NP_001244127.1:n.*940C>T
NM_003590.4:c.*940C>T	NP_003581.1:n.*940C>T
XM_006712800.2:c.*940C>T	XP_006712863.2:n.*940C>T
XM_011511994.1:c.*940C>T	XP_011510296.1:n.*940C>T
XM_011511995.1:c.*940C>T	XP_011510297.1:n.*940C>T
XM_011511996.1:c.*940C>T	XP_011510298.1:n.*940C>T
XM_011511997.1:c.*940C>T	XP_011510299.1:n.*940C>T
XM_011511994.3:c.*940C>T	XP_011510296.1:n.*940C>T
XM_011511996.2:c.*940C>T	XP_011510298.1:n.*940C>T
NM_003590.5:c.*940C>T MANE Select	NP_003581.1:n.*940C>T
NM_001257198.2:c.*940C>T	NP_001244127.1:n.*940C>T
NM_001257197.2:c.*940C>T	NP_001244126.1:n.*940C>T