Canonical Allele Identifier: CA350827521

Gene: CUL3

Linked Data

• gnomAD v4: 2-224503753-C-A
• MyVariant Identifiers: chr2:g.225368470C>A (hg19) ; chr2:g.224503753C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503753C>A , CM000664.2:g.224503753C>A	GRCh38
NC_000002.11:g.225368470C>A , CM000664.1:g.225368470C>A	GRCh37
NC_000002.10:g.225076714C>A	NCBI36
NG_032169.1:g.86645G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1276G>T MANE Select	ENSP00000264414.4:p.Asp426Tyr
ENST00000264414.8:c.1276G>T	ENSP00000264414.4:p.Asp426Tyr
ENST00000344951.8:c.1078G>T	ENSP00000343601.4:p.Asp360Tyr
ENST00000409096.5:c.1204G>T	ENSP00000387200.1:p.Asp402Tyr
ENST00000409777.5:c.1204G>T	ENSP00000386525.1:p.Asp402Tyr
ENST00000481135.1:n.572G>T
ENST00000617432.4:c.-1G>T	ENSP00000477851.1:n.-1G>T
NM_001257197.1:c.1078G>T	NP_001244126.1:p.Asp360Tyr
NM_001257198.1:c.1294G>T	NP_001244127.1:p.Asp432Tyr
NM_003590.4:c.1276G>T	NP_003581.1:p.Asp426Tyr
XM_006712800.2:c.1243G>T	XP_006712863.2:p.Asp415Tyr
XM_011511994.1:c.1129G>T	XP_011510296.1:p.Asp377Tyr
XM_011511995.1:c.1234G>T	XP_011510297.1:p.Asp412Tyr
XM_011511996.1:c.1084G>T	XP_011510298.1:p.Asp362Tyr
XM_011511997.1:c.976G>T	XP_011510299.1:p.Asp326Tyr
XM_011511994.3:c.1129G>T	XP_011510296.1:p.Asp377Tyr
XM_011511996.2:c.1084G>T	XP_011510298.1:p.Asp362Tyr
NM_003590.5:c.1276G>T MANE Select	NP_003581.1:p.Asp426Tyr
NM_001257198.2:c.1294G>T	NP_001244127.1:p.Asp432Tyr
NM_001257197.2:c.1078G>T	NP_001244126.1:p.Asp360Tyr