Canonical Allele Identifier: CA9428837
Gene: ZFP36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39408124G>A , CM000681.2:g.39408124G>A GRCh38
NC_000019.9:g.39898764G>A , CM000681.1:g.39898764G>A GRCh37
NC_000019.8:g.44590604G>A NCBI36
NG_054904.1:g.543G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000594045.2:c.*389G>A ENSP00000472329.2:n.*389G>A
ENST00000594442.2:c.424G>A ENSP00000471239.2:p.Ala142Thr
ENST00000597629.3:c.406G>A MANE Select ENSP00000469647.2:p.Ala136Thr
ENST00000652583.1:n.455G>A
ENST00000594045.1:c.*389G>A ENSP00000472329.1:n.*389G>A
ENST00000594442.1:c.455G>A
ENST00000597629.1:c.424G>A ENSP00000469647.1:p.Ala142Thr
ENST00000600033.1:c.425G>A
NM_003407.3:c.424G>A NP_003398.2:p.Ala142Thr
NM_003407.4:c.406G>A NP_003398.3:p.Ala136Thr
NM_003407.5:c.406G>A MANE Select NP_003398.3:p.Ala136Thr