Canonical Allele Identifier: CA431492701

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197206
• MyVariant Identifiers: chr2:g.225368471T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503754T>C , CM000664.2:g.224503754T>C	GRCh38
NC_000002.11:g.225368471T>C , CM000664.1:g.225368471T>C	GRCh37
NC_000002.10:g.225076715T>C	NCBI36
NG_032169.1:g.86644A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1275A>G MANE Select	ENSP00000264414.4:p.Lys425=
ENST00000264414.8:c.1275A>G	ENSP00000264414.4:p.Lys425=
ENST00000344951.8:c.1077A>G	ENSP00000343601.4:p.Lys359=
ENST00000409096.5:c.1203A>G	ENSP00000387200.1:p.Lys401=
ENST00000409777.5:c.1203A>G	ENSP00000386525.1:p.Lys401=
ENST00000481135.1:n.571A>G
ENST00000617432.4:c.-2A>G	ENSP00000477851.1:n.-2A>G
NM_001257197.1:c.1077A>G	NP_001244126.1:p.Lys359=
NM_001257198.1:c.1293A>G	NP_001244127.1:p.Lys431=
NM_003590.4:c.1275A>G	NP_003581.1:p.Lys425=
XM_006712800.2:c.1242A>G	XP_006712863.2:p.Lys414=
XM_011511994.1:c.1128A>G	XP_011510296.1:p.Lys376=
XM_011511995.1:c.1233A>G	XP_011510297.1:p.Lys411=
XM_011511996.1:c.1083A>G	XP_011510298.1:p.Lys361=
XM_011511997.1:c.975A>G	XP_011510299.1:p.Lys325=
XM_011511994.3:c.1128A>G	XP_011510296.1:p.Lys376=
XM_011511996.2:c.1083A>G	XP_011510298.1:p.Lys361=
NM_003590.5:c.1275A>G MANE Select	NP_003581.1:p.Lys425=
NM_001257198.2:c.1293A>G	NP_001244127.1:p.Lys431=
NM_001257197.2:c.1077A>G	NP_001244126.1:p.Lys359=