Canonical Allele Identifier: CA431492737

Gene: CUL3

Linked Data

• dbSNP Id: rs754817876
• MyVariant Identifiers: chr2:g.225368537T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503820T>A , CM000664.2:g.224503820T>A	GRCh38
NC_000002.11:g.225368537T>A , CM000664.1:g.225368537T>A	GRCh37
NC_000002.10:g.225076781T>A	NCBI36
NG_032169.1:g.86578A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1209A>T MANE Select	ENSP00000264414.4:p.Leu403=
ENST00000264414.8:c.1209A>T	ENSP00000264414.4:p.Leu403=
ENST00000344951.8:c.1011A>T	ENSP00000343601.4:p.Leu337=
ENST00000409096.5:c.1137A>T	ENSP00000387200.1:p.Leu379=
ENST00000409777.5:c.1137A>T	ENSP00000386525.1:p.Leu379=
ENST00000481135.1:n.505A>T
ENST00000617432.4:c.-68A>T	ENSP00000477851.1:n.-68A>T
NM_001257197.1:c.1011A>T	NP_001244126.1:p.Leu337=
NM_001257198.1:c.1227A>T	NP_001244127.1:p.Leu409=
NM_003590.4:c.1209A>T	NP_003581.1:p.Leu403=
XM_006712800.2:c.1176A>T	XP_006712863.2:p.Leu392=
XM_011511994.1:c.1062A>T	XP_011510296.1:p.Leu354=
XM_011511995.1:c.1167A>T	XP_011510297.1:p.Leu389=
XM_011511996.1:c.1017A>T	XP_011510298.1:p.Leu339=
XM_011511997.1:c.909A>T	XP_011510299.1:p.Leu303=
XM_011511994.3:c.1062A>T	XP_011510296.1:p.Leu354=
XM_011511996.2:c.1017A>T	XP_011510298.1:p.Leu339=
NM_003590.5:c.1209A>T MANE Select	NP_003581.1:p.Leu403=
NM_001257198.2:c.1227A>T	NP_001244127.1:p.Leu409=
NM_001257197.2:c.1011A>T	NP_001244126.1:p.Leu337=