Canonical Allele Identifier: CA431492553

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368372T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503655T>C , CM000664.2:g.224503655T>C	GRCh38
NC_000002.11:g.225368372T>C , CM000664.1:g.225368372T>C	GRCh37
NC_000002.10:g.225076616T>C	NCBI36
NG_032169.1:g.86743A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1374A>G MANE Select	ENSP00000264414.4:p.Leu458=
ENST00000264414.8:c.1374A>G	ENSP00000264414.4:p.Leu458=
ENST00000344951.8:c.1176A>G	ENSP00000343601.4:p.Leu392=
ENST00000409096.5:c.1302A>G	ENSP00000387200.1:p.Leu434=
ENST00000409777.5:c.1302A>G	ENSP00000386525.1:p.Leu434=
ENST00000481135.1:n.670A>G
ENST00000617432.4:c.96A>G	ENSP00000477851.1:p.Leu32=
NM_001257197.1:c.1176A>G	NP_001244126.1:p.Leu392=
NM_001257198.1:c.1392A>G	NP_001244127.1:p.Leu464=
NM_003590.4:c.1374A>G	NP_003581.1:p.Leu458=
XM_006712800.2:c.1341A>G	XP_006712863.2:p.Leu447=
XM_011511994.1:c.1227A>G	XP_011510296.1:p.Leu409=
XM_011511995.1:c.1332A>G	XP_011510297.1:p.Leu444=
XM_011511996.1:c.1182A>G	XP_011510298.1:p.Leu394=
XM_011511997.1:c.1074A>G	XP_011510299.1:p.Leu358=
XM_011511994.3:c.1227A>G	XP_011510296.1:p.Leu409=
XM_011511996.2:c.1182A>G	XP_011510298.1:p.Leu394=
NM_003590.5:c.1374A>G MANE Select	NP_003581.1:p.Leu458=
NM_001257198.2:c.1392A>G	NP_001244127.1:p.Leu464=
NM_001257197.2:c.1176A>G	NP_001244126.1:p.Leu392=