Canonical Allele Identifier: CA431492713
Gene: CUL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.225368492A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503775A>T , CM000664.2:g.224503775A>T GRCh38
NC_000002.11:g.225368492A>T , CM000664.1:g.225368492A>T GRCh37
NC_000002.10:g.225076736A>T NCBI36
NG_032169.1:g.86623T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1254T>A MANE Select ENSP00000264414.4:p.Leu418=
ENST00000264414.8:c.1254T>A ENSP00000264414.4:p.Leu418=
ENST00000344951.8:c.1056T>A ENSP00000343601.4:p.Leu352=
ENST00000409096.5:c.1182T>A ENSP00000387200.1:p.Leu394=
ENST00000409777.5:c.1182T>A ENSP00000386525.1:p.Leu394=
ENST00000481135.1:n.550T>A
ENST00000617432.4:c.-23T>A ENSP00000477851.1:n.-23T>A
NM_001257197.1:c.1056T>A NP_001244126.1:p.Leu352=
NM_001257198.1:c.1272T>A NP_001244127.1:p.Leu424=
NM_003590.4:c.1254T>A NP_003581.1:p.Leu418=
XM_006712800.2:c.1221T>A XP_006712863.2:p.Leu407=
XM_011511994.1:c.1107T>A XP_011510296.1:p.Leu369=
XM_011511995.1:c.1212T>A XP_011510297.1:p.Leu404=
XM_011511996.1:c.1062T>A XP_011510298.1:p.Leu354=
XM_011511997.1:c.954T>A XP_011510299.1:p.Leu318=
XM_011511994.3:c.1107T>A XP_011510296.1:p.Leu369=
XM_011511996.2:c.1062T>A XP_011510298.1:p.Leu354=
NM_003590.5:c.1254T>A MANE Select NP_003581.1:p.Leu418=
NM_001257198.2:c.1272T>A NP_001244127.1:p.Leu424=
NM_001257197.2:c.1056T>A NP_001244126.1:p.Leu352=