Canonical Allele Identifier: CA431492715

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197381
• MyVariant Identifiers: chr2:g.225368495G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503778G>A , CM000664.2:g.224503778G>A	GRCh38
NC_000002.11:g.225368495G>A , CM000664.1:g.225368495G>A	GRCh37
NC_000002.10:g.225076739G>A	NCBI36
NG_032169.1:g.86620C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1251C>T MANE Select	ENSP00000264414.4:p.Val417=
ENST00000264414.8:c.1251C>T	ENSP00000264414.4:p.Val417=
ENST00000344951.8:c.1053C>T	ENSP00000343601.4:p.Val351=
ENST00000409096.5:c.1179C>T	ENSP00000387200.1:p.Val393=
ENST00000409777.5:c.1179C>T	ENSP00000386525.1:p.Val393=
ENST00000481135.1:n.547C>T
ENST00000617432.4:c.-26C>T	ENSP00000477851.1:n.-26C>T
NM_001257197.1:c.1053C>T	NP_001244126.1:p.Val351=
NM_001257198.1:c.1269C>T	NP_001244127.1:p.Val423=
NM_003590.4:c.1251C>T	NP_003581.1:p.Val417=
XM_006712800.2:c.1218C>T	XP_006712863.2:p.Val406=
XM_011511994.1:c.1104C>T	XP_011510296.1:p.Val368=
XM_011511995.1:c.1209C>T	XP_011510297.1:p.Val403=
XM_011511996.1:c.1059C>T	XP_011510298.1:p.Val353=
XM_011511997.1:c.951C>T	XP_011510299.1:p.Val317=
XM_011511994.3:c.1104C>T	XP_011510296.1:p.Val368=
XM_011511996.2:c.1059C>T	XP_011510298.1:p.Val353=
NM_003590.5:c.1251C>T MANE Select	NP_003581.1:p.Val417=
NM_001257198.2:c.1269C>T	NP_001244127.1:p.Val423=
NM_001257197.2:c.1053C>T	NP_001244126.1:p.Val351=