Canonical Allele Identifier: CA1331555857
Gene: CUL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503553C= , CM000664.2:g.224503553C= GRCh38
NC_000002.11:g.225368270C= , CM000664.1:g.225368270C= GRCh37
NC_000002.10:g.225076514C= NCBI36
NG_032169.1:g.86845G=

Transcript Alleles

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