Canonical Allele Identifier: CA269963

Gene: CUL3

Linked Data

• ClinVar Variation Id: 100523
• ClinVar RCV Id: RCV000128495
• dbSNP Id: rs199469657
• MyVariant Identifiers: chr2:g.225368365_225368370del (hg19) ; chr2:g.224503648_224503653del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503651_224503656del , CM000664.2:g.224503651_224503656del	GRCh38
NC_000002.11:g.225368368_225368373del , CM000664.1:g.225368368_225368373del	GRCh37
NC_000002.10:g.225076612_225076617del	NCBI36
NG_032169.1:g.86745_86750del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1376_1377+4del
ENST00000264414.8:c.1376_1377+4del
ENST00000344951.8:c.1178_1179+4del
ENST00000409096.5:c.1304_1305+4del
ENST00000409777.5:c.1304_1305+4del
ENST00000481135.1:n.672_673+4del
ENST00000617432.4:c.98_99+4del
NM_001257197.1:c.1178_1179+4del
NM_001257198.1:c.1394_1395+4del
NM_003590.4:c.1376_1377+4del
XM_006712800.2:c.1343_1344+4del
XM_011511994.1:c.1229_1230+4del
XM_011511995.1:c.1334_1335+4del
XM_011511996.1:c.1184_1185+4del
XM_011511997.1:c.1076_1077+4del
XM_011511994.3:c.1229_1230+4del
XM_011511996.2:c.1184_1185+4del
NM_003590.5:c.1376_1377+4del
NM_001257198.2:c.1394_1395+4del
NM_001257197.2:c.1178_1179+4del