Canonical Allele Identifier: CA765436365

Gene: CUL3

Linked Data

• dbSNP Id: rs1218045729
• gnomAD v3: 2-224503559-A-C
• gnomAD v4: 2-224503559-A-C
• MyVariant Identifiers: chr2:g.225368276A>C (hg19) ; chr2:g.224503559A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503559A>C , CM000664.2:g.224503559A>C	GRCh38
NC_000002.11:g.225368276A>C , CM000664.1:g.225368276A>C	GRCh37
NC_000002.10:g.225076520A>C	NCBI36
NG_032169.1:g.86839T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1377+93T>G MANE Select	ENSP00000264414.4:n.1377+93T>G
ENST00000264414.8:c.1377+93T>G	ENSP00000264414.4:n.1377+93T>G
ENST00000344951.8:c.1179+93T>G	ENSP00000343601.4:n.1179+93T>G
ENST00000409096.5:c.1305+93T>G	ENSP00000387200.1:n.1305+93T>G
ENST00000409777.5:c.1305+93T>G	ENSP00000386525.1:n.1305+93T>G
ENST00000481135.1:n.673+93T>G
ENST00000617432.4:c.99+93T>G	ENSP00000477851.1:n.99+93T>G
NM_001257197.1:c.1179+93T>G	NP_001244126.1:n.1179+93T>G
NM_001257198.1:c.1395+93T>G	NP_001244127.1:n.1395+93T>G
NM_003590.4:c.1377+93T>G	NP_003581.1:n.1377+93T>G
XM_006712800.2:c.1344+93T>G	XP_006712863.2:n.1344+93T>G
XM_011511994.1:c.1230+93T>G	XP_011510296.1:n.1230+93T>G
XM_011511995.1:c.1335+93T>G	XP_011510297.1:n.1335+93T>G
XM_011511996.1:c.1185+93T>G	XP_011510298.1:n.1185+93T>G
XM_011511997.1:c.1077+93T>G	XP_011510299.1:n.1077+93T>G
XM_011511994.3:c.1230+93T>G	XP_011510296.1:n.1230+93T>G
XM_011511996.2:c.1185+93T>G	XP_011510298.1:n.1185+93T>G
NM_003590.5:c.1377+93T>G MANE Select	NP_003581.1:n.1377+93T>G
NM_001257198.2:c.1395+93T>G	NP_001244127.1:n.1395+93T>G
NM_001257197.2:c.1179+93T>G	NP_001244126.1:n.1179+93T>G