Canonical Allele Identifier: CA350826942

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368385A>G (hg19) ; chr2:g.224503668A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503668A>G , CM000664.2:g.224503668A>G	GRCh38
NC_000002.11:g.225368385A>G , CM000664.1:g.225368385A>G	GRCh37
NC_000002.10:g.225076629A>G	NCBI36
NG_032169.1:g.86730T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1361T>C MANE Select	ENSP00000264414.4:p.Met454Thr
ENST00000264414.8:c.1361T>C	ENSP00000264414.4:p.Met454Thr
ENST00000344951.8:c.1163T>C	ENSP00000343601.4:p.Met388Thr
ENST00000409096.5:c.1289T>C	ENSP00000387200.1:p.Met430Thr
ENST00000409777.5:c.1289T>C	ENSP00000386525.1:p.Met430Thr
ENST00000481135.1:n.657T>C
ENST00000617432.4:c.83T>C	ENSP00000477851.1:p.Met28Thr
NM_001257197.1:c.1163T>C	NP_001244126.1:p.Met388Thr
NM_001257198.1:c.1379T>C	NP_001244127.1:p.Met460Thr
NM_003590.4:c.1361T>C	NP_003581.1:p.Met454Thr
XM_006712800.2:c.1328T>C	XP_006712863.2:p.Met443Thr
XM_011511994.1:c.1214T>C	XP_011510296.1:p.Met405Thr
XM_011511995.1:c.1319T>C	XP_011510297.1:p.Met440Thr
XM_011511996.1:c.1169T>C	XP_011510298.1:p.Met390Thr
XM_011511997.1:c.1061T>C	XP_011510299.1:p.Met354Thr
XM_011511994.3:c.1214T>C	XP_011510296.1:p.Met405Thr
XM_011511996.2:c.1169T>C	XP_011510298.1:p.Met390Thr
NM_003590.5:c.1361T>C MANE Select	NP_003581.1:p.Met454Thr
NM_001257198.2:c.1379T>C	NP_001244127.1:p.Met460Thr
NM_001257197.2:c.1163T>C	NP_001244126.1:p.Met388Thr