Canonical Allele Identifier: CA431492707

Gene: CUL3

Linked Data

• dbSNP Id: rs749893181
• MyVariant Identifiers: chr2:g.225368483A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503766A>G , CM000664.2:g.224503766A>G	GRCh38
NC_000002.11:g.225368483A>G , CM000664.1:g.225368483A>G	GRCh37
NC_000002.10:g.225076727A>G	NCBI36
NG_032169.1:g.86632T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1263T>C MANE Select	ENSP00000264414.4:p.Phe421=
ENST00000264414.8:c.1263T>C	ENSP00000264414.4:p.Phe421=
ENST00000344951.8:c.1065T>C	ENSP00000343601.4:p.Phe355=
ENST00000409096.5:c.1191T>C	ENSP00000387200.1:p.Phe397=
ENST00000409777.5:c.1191T>C	ENSP00000386525.1:p.Phe397=
ENST00000481135.1:n.559T>C
ENST00000617432.4:c.-14T>C	ENSP00000477851.1:n.-14T>C
NM_001257197.1:c.1065T>C	NP_001244126.1:p.Phe355=
NM_001257198.1:c.1281T>C	NP_001244127.1:p.Phe427=
NM_003590.4:c.1263T>C	NP_003581.1:p.Phe421=
XM_006712800.2:c.1230T>C	XP_006712863.2:p.Phe410=
XM_011511994.1:c.1116T>C	XP_011510296.1:p.Phe372=
XM_011511995.1:c.1221T>C	XP_011510297.1:p.Phe407=
XM_011511996.1:c.1071T>C	XP_011510298.1:p.Phe357=
XM_011511997.1:c.963T>C	XP_011510299.1:p.Phe321=
XM_011511994.3:c.1116T>C	XP_011510296.1:p.Phe372=
XM_011511996.2:c.1071T>C	XP_011510298.1:p.Phe357=
NM_003590.5:c.1263T>C MANE Select	NP_003581.1:p.Phe421=
NM_001257198.2:c.1281T>C	NP_001244127.1:p.Phe427=
NM_001257197.2:c.1065T>C	NP_001244126.1:p.Phe355=