Canonical Allele Identifier: CA350827608

Gene: CUL3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1250T>C MANE Select	ENSP00000264414.4:p.Val417Ala
ENST00000264414.8:c.1250T>C	ENSP00000264414.4:p.Val417Ala
ENST00000344951.8:c.1052T>C	ENSP00000343601.4:p.Val351Ala
ENST00000409096.5:c.1178T>C	ENSP00000387200.1:p.Val393Ala
ENST00000409777.5:c.1178T>C	ENSP00000386525.1:p.Val393Ala
ENST00000481135.1:n.546T>C
ENST00000617432.4:c.-27T>C	ENSP00000477851.1:n.-27T>C
NM_001257197.1:c.1052T>C	NP_001244126.1:p.Val351Ala
NM_001257198.1:c.1268T>C	NP_001244127.1:p.Val423Ala
NM_003590.4:c.1250T>C	NP_003581.1:p.Val417Ala
XM_006712800.2:c.1217T>C	XP_006712863.2:p.Val406Ala
XM_011511994.1:c.1103T>C	XP_011510296.1:p.Val368Ala
XM_011511995.1:c.1208T>C	XP_011510297.1:p.Val403Ala
XM_011511996.1:c.1058T>C	XP_011510298.1:p.Val353Ala
XM_011511997.1:c.950T>C	XP_011510299.1:p.Val317Ala
XM_011511994.3:c.1103T>C	XP_011510296.1:p.Val368Ala
XM_011511996.2:c.1058T>C	XP_011510298.1:p.Val353Ala
NM_003590.5:c.1250T>C MANE Select	NP_003581.1:p.Val417Ala
NM_001257198.2:c.1268T>C	NP_001244127.1:p.Val423Ala
NM_001257197.2:c.1052T>C	NP_001244126.1:p.Val351Ala