Canonical Allele Identifier: CA431492708

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197304
• gnomAD v4: 2-224503769-C-T
• MyVariant Identifiers: chr2:g.225368486C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503769C>T , CM000664.2:g.224503769C>T	GRCh38
NC_000002.11:g.225368486C>T , CM000664.1:g.225368486C>T	GRCh37
NC_000002.10:g.225076730C>T	NCBI36
NG_032169.1:g.86629G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1260G>A MANE Select	ENSP00000264414.4:p.Arg420=
ENST00000264414.8:c.1260G>A	ENSP00000264414.4:p.Arg420=
ENST00000344951.8:c.1062G>A	ENSP00000343601.4:p.Arg354=
ENST00000409096.5:c.1188G>A	ENSP00000387200.1:p.Arg396=
ENST00000409777.5:c.1188G>A	ENSP00000386525.1:p.Arg396=
ENST00000481135.1:n.556G>A
ENST00000617432.4:c.-17G>A	ENSP00000477851.1:n.-17G>A
NM_001257197.1:c.1062G>A	NP_001244126.1:p.Arg354=
NM_001257198.1:c.1278G>A	NP_001244127.1:p.Arg426=
NM_003590.4:c.1260G>A	NP_003581.1:p.Arg420=
XM_006712800.2:c.1227G>A	XP_006712863.2:p.Arg409=
XM_011511994.1:c.1113G>A	XP_011510296.1:p.Arg371=
XM_011511995.1:c.1218G>A	XP_011510297.1:p.Arg406=
XM_011511996.1:c.1068G>A	XP_011510298.1:p.Arg356=
XM_011511997.1:c.960G>A	XP_011510299.1:p.Arg320=
XM_011511994.3:c.1113G>A	XP_011510296.1:p.Arg371=
XM_011511996.2:c.1068G>A	XP_011510298.1:p.Arg356=
NM_003590.5:c.1260G>A MANE Select	NP_003581.1:p.Arg420=
NM_001257198.2:c.1278G>A	NP_001244127.1:p.Arg426=
NM_001257197.2:c.1062G>A	NP_001244126.1:p.Arg354=