Canonical Allele Identifier: CA405783774
Gene: ZFP36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39408005C>A , CM000681.2:g.39408005C>A GRCh38
NC_000019.9:g.39898645C>A , CM000681.1:g.39898645C>A GRCh37
NC_000019.8:g.44590485C>A NCBI36
NG_054904.1:g.424C>A

Transcript Alleles

HGVS Amino-acid Change
NM_003407.5:c.287C>A MANE Select NP_003398.3:p.Ala96Glu
ENST00000597629.3:c.287C>A MANE Select ENSP00000469647.2:p.Ala96Glu
NM_003407.3:c.305C>A NP_003398.2:p.Ala102Glu
NM_003407.4:c.287C>A NP_003398.3:p.Ala96Glu
ENST00000594045.1:c.*270C>A ENSP00000472329.1:n.*270C>A
ENST00000594045.2:c.*270C>A ENSP00000472329.2:n.*270C>A
ENST00000594442.1:c.336C>A
ENST00000594442.2:c.305C>A ENSP00000471239.2:p.Ala102Glu
ENST00000597629.1:c.305C>A ENSP00000469647.1:p.Ala102Glu
ENST00000600033.1:c.306C>A
ENST00000652583.1:n.336C>A