Canonical Allele Identifier: CA350827404
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503730T>C , CM000664.2:g.224503730T>C GRCh38
NC_000002.11:g.225368447T>C , CM000664.1:g.225368447T>C GRCh37
NC_000002.10:g.225076691T>C NCBI36
NG_032169.1:g.86668A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1299A>G MANE Select ENSP00000264414.4:p.Lys433=
ENST00000264414.8:c.1299A>G ENSP00000264414.4:p.Lys433=
ENST00000344951.8:c.1101A>G ENSP00000343601.4:p.Lys367=
ENST00000409096.5:c.1227A>G ENSP00000387200.1:p.Lys409=
ENST00000409777.5:c.1227A>G ENSP00000386525.1:p.Lys409=
ENST00000481135.1:n.595A>G
ENST00000617432.4:c.23A>G ENSP00000477851.1:p.Asn8Ser
NM_001257197.1:c.1101A>G NP_001244126.1:p.Lys367=
NM_001257198.1:c.1317A>G NP_001244127.1:p.Lys439=
NM_003590.4:c.1299A>G NP_003581.1:p.Lys433=
XM_006712800.2:c.1266A>G XP_006712863.2:p.Lys422=
XM_011511994.1:c.1152A>G XP_011510296.1:p.Lys384=
XM_011511995.1:c.1257A>G XP_011510297.1:p.Lys419=
XM_011511996.1:c.1107A>G XP_011510298.1:p.Lys369=
XM_011511997.1:c.999A>G XP_011510299.1:p.Lys333=
XM_011511994.3:c.1152A>G XP_011510296.1:p.Lys384=
XM_011511996.2:c.1107A>G XP_011510298.1:p.Lys369=
NM_003590.5:c.1299A>G MANE Select NP_003581.1:p.Lys433=
NM_001257198.2:c.1317A>G NP_001244127.1:p.Lys439=
NM_001257197.2:c.1101A>G NP_001244126.1:p.Lys367=