Canonical Allele Identifier: CA350826909

Gene: CUL3

Linked Data

• dbSNP Id: rs1692484584
• gnomAD v4: 2-224503662-G-A
• MyVariant Identifiers: chr2:g.225368379G>A (hg19) ; chr2:g.224503662G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503662G>A , CM000664.2:g.224503662G>A	GRCh38
NC_000002.11:g.225368379G>A , CM000664.1:g.225368379G>A	GRCh37
NC_000002.10:g.225076623G>A	NCBI36
NG_032169.1:g.86736C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1367C>T MANE Select	ENSP00000264414.4:p.Ser456Phe
ENST00000264414.8:c.1367C>T	ENSP00000264414.4:p.Ser456Phe
ENST00000344951.8:c.1169C>T	ENSP00000343601.4:p.Ser390Phe
ENST00000409096.5:c.1295C>T	ENSP00000387200.1:p.Ser432Phe
ENST00000409777.5:c.1295C>T	ENSP00000386525.1:p.Ser432Phe
ENST00000481135.1:n.663C>T
ENST00000617432.4:c.89C>T	ENSP00000477851.1:p.Ser30Phe
NM_001257197.1:c.1169C>T	NP_001244126.1:p.Ser390Phe
NM_001257198.1:c.1385C>T	NP_001244127.1:p.Ser462Phe
NM_003590.4:c.1367C>T	NP_003581.1:p.Ser456Phe
XM_006712800.2:c.1334C>T	XP_006712863.2:p.Ser445Phe
XM_011511994.1:c.1220C>T	XP_011510296.1:p.Ser407Phe
XM_011511995.1:c.1325C>T	XP_011510297.1:p.Ser442Phe
XM_011511996.1:c.1175C>T	XP_011510298.1:p.Ser392Phe
XM_011511997.1:c.1067C>T	XP_011510299.1:p.Ser356Phe
XM_011511994.3:c.1220C>T	XP_011510296.1:p.Ser407Phe
XM_011511996.2:c.1175C>T	XP_011510298.1:p.Ser392Phe
NM_003590.5:c.1367C>T MANE Select	NP_003581.1:p.Ser456Phe
NM_001257198.2:c.1385C>T	NP_001244127.1:p.Ser462Phe
NM_001257197.2:c.1169C>T	NP_001244126.1:p.Ser390Phe