Canonical Allele Identifier: CA350827538

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368477T>A (hg19) ; chr2:g.224503760T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503760T>A , CM000664.2:g.224503760T>A	GRCh38
NC_000002.11:g.225368477T>A , CM000664.1:g.225368477T>A	GRCh37
NC_000002.10:g.225076721T>A	NCBI36
NG_032169.1:g.86638A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1269A>T MANE Select	ENSP00000264414.4:p.Gln423His
ENST00000264414.8:c.1269A>T	ENSP00000264414.4:p.Gln423His
ENST00000344951.8:c.1071A>T	ENSP00000343601.4:p.Gln357His
ENST00000409096.5:c.1197A>T	ENSP00000387200.1:p.Gln399His
ENST00000409777.5:c.1197A>T	ENSP00000386525.1:p.Gln399His
ENST00000481135.1:n.565A>T
ENST00000617432.4:c.-8A>T	ENSP00000477851.1:n.-8A>T
NM_001257197.1:c.1071A>T	NP_001244126.1:p.Gln357His
NM_001257198.1:c.1287A>T	NP_001244127.1:p.Gln429His
NM_003590.4:c.1269A>T	NP_003581.1:p.Gln423His
XM_006712800.2:c.1236A>T	XP_006712863.2:p.Gln412His
XM_011511994.1:c.1122A>T	XP_011510296.1:p.Gln374His
XM_011511995.1:c.1227A>T	XP_011510297.1:p.Gln409His
XM_011511996.1:c.1077A>T	XP_011510298.1:p.Gln359His
XM_011511997.1:c.969A>T	XP_011510299.1:p.Gln323His
XM_011511994.3:c.1122A>T	XP_011510296.1:p.Gln374His
XM_011511996.2:c.1077A>T	XP_011510298.1:p.Gln359His
NM_003590.5:c.1269A>T MANE Select	NP_003581.1:p.Gln423His
NM_001257198.2:c.1287A>T	NP_001244127.1:p.Gln429His
NM_001257197.2:c.1071A>T	NP_001244126.1:p.Gln357His