Canonical Allele Identifier: CA350827129

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368412C>G (hg19) ; chr2:g.224503695C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503695C>G , CM000664.2:g.224503695C>G	GRCh38
NC_000002.11:g.225368412C>G , CM000664.1:g.225368412C>G	GRCh37
NC_000002.10:g.225076656C>G	NCBI36
NG_032169.1:g.86703G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1334G>C MANE Select	ENSP00000264414.4:p.Ser445Thr
ENST00000264414.8:c.1334G>C	ENSP00000264414.4:p.Ser445Thr
ENST00000344951.8:c.1136G>C	ENSP00000343601.4:p.Ser379Thr
ENST00000409096.5:c.1262G>C	ENSP00000387200.1:p.Ser421Thr
ENST00000409777.5:c.1262G>C	ENSP00000386525.1:p.Ser421Thr
ENST00000481135.1:n.630G>C
ENST00000617432.4:c.58G>C	ENSP00000477851.1:p.Val20Leu
NM_001257197.1:c.1136G>C	NP_001244126.1:p.Ser379Thr
NM_001257198.1:c.1352G>C	NP_001244127.1:p.Ser451Thr
NM_003590.4:c.1334G>C	NP_003581.1:p.Ser445Thr
XM_006712800.2:c.1301G>C	XP_006712863.2:p.Ser434Thr
XM_011511994.1:c.1187G>C	XP_011510296.1:p.Ser396Thr
XM_011511995.1:c.1292G>C	XP_011510297.1:p.Ser431Thr
XM_011511996.1:c.1142G>C	XP_011510298.1:p.Ser381Thr
XM_011511997.1:c.1034G>C	XP_011510299.1:p.Ser345Thr
XM_011511994.3:c.1187G>C	XP_011510296.1:p.Ser396Thr
XM_011511996.2:c.1142G>C	XP_011510298.1:p.Ser381Thr
NM_003590.5:c.1334G>C MANE Select	NP_003581.1:p.Ser445Thr
NM_001257198.2:c.1352G>C	NP_001244127.1:p.Ser451Thr
NM_001257197.2:c.1136G>C	NP_001244126.1:p.Ser379Thr