Canonical Allele Identifier: CA269964

Gene: CUL3

Linked Data

• ClinVar Variation Id: 100524
• ClinVar RCV Id: RCV000128496
• dbSNP Id: rs199469659

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503652dup , CM000664.2:g.224503652dup	GRCh38
NC_000002.11:g.225368369dup , CM000664.1:g.225368369dup	GRCh37
NC_000002.10:g.225076613dup	NCBI36
NG_032169.1:g.86747dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1377+1dup
ENST00000264414.8:c.1377+1dup
ENST00000344951.8:c.1179+1dup
ENST00000409096.5:c.1305+1dup
ENST00000409777.5:c.1305+1dup
ENST00000481135.1:n.673+1dup
ENST00000617432.4:c.99+1dup
NM_001257197.1:c.1179+1dup
NM_001257198.1:c.1395+1dup
NM_003590.4:c.1377+1dup
XM_006712800.2:c.1344+1dup
XM_011511994.1:c.1230+1dup
XM_011511995.1:c.1335+1dup
XM_011511996.1:c.1185+1dup
XM_011511997.1:c.1077+1dup
XM_011511994.3:c.1230+1dup
XM_011511996.2:c.1185+1dup
NM_003590.5:c.1377+1dup
NM_001257198.2:c.1395+1dup
NM_001257197.2:c.1179+1dup