Canonical Allele Identifier: CA350827612

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368496A>C (hg19) ; chr2:g.224503779A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503779A>C , CM000664.2:g.224503779A>C	GRCh38
NC_000002.11:g.225368496A>C , CM000664.1:g.225368496A>C	GRCh37
NC_000002.10:g.225076740A>C	NCBI36
NG_032169.1:g.86619T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1250T>G MANE Select	ENSP00000264414.4:p.Val417Gly
ENST00000264414.8:c.1250T>G	ENSP00000264414.4:p.Val417Gly
ENST00000344951.8:c.1052T>G	ENSP00000343601.4:p.Val351Gly
ENST00000409096.5:c.1178T>G	ENSP00000387200.1:p.Val393Gly
ENST00000409777.5:c.1178T>G	ENSP00000386525.1:p.Val393Gly
ENST00000481135.1:n.546T>G
ENST00000617432.4:c.-27T>G	ENSP00000477851.1:n.-27T>G
NM_001257197.1:c.1052T>G	NP_001244126.1:p.Val351Gly
NM_001257198.1:c.1268T>G	NP_001244127.1:p.Val423Gly
NM_003590.4:c.1250T>G	NP_003581.1:p.Val417Gly
XM_006712800.2:c.1217T>G	XP_006712863.2:p.Val406Gly
XM_011511994.1:c.1103T>G	XP_011510296.1:p.Val368Gly
XM_011511995.1:c.1208T>G	XP_011510297.1:p.Val403Gly
XM_011511996.1:c.1058T>G	XP_011510298.1:p.Val353Gly
XM_011511997.1:c.950T>G	XP_011510299.1:p.Val317Gly
XM_011511994.3:c.1103T>G	XP_011510296.1:p.Val368Gly
XM_011511996.2:c.1058T>G	XP_011510298.1:p.Val353Gly
NM_003590.5:c.1250T>G MANE Select	NP_003581.1:p.Val417Gly
NM_001257198.2:c.1268T>G	NP_001244127.1:p.Val423Gly
NM_001257197.2:c.1052T>G	NP_001244126.1:p.Val351Gly