Canonical Allele Identifier: CA269966
Gene: CUL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 100526
ClinVar RCV Id: RCV000128498
dbSNP Id: rs199469661
MyVariant Identifiers: chr2:g.225368366T>C (hg19) chr2:g.224503649T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503649T>C , CM000664.2:g.224503649T>C GRCh38
NC_000002.11:g.225368366T>C , CM000664.1:g.225368366T>C GRCh37
NC_000002.10:g.225076610T>C NCBI36
NG_032169.1:g.86749A>G

Transcript Alleles

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