Human (GRCh38.p14)
Description

myomesin 1 [Source:HGNC Symbol;Acc:HGNC:7613]

Location
About this transcript

This transcript has 38 exons, is annotated with 106 domains and features, is associated with 65433 variant alleles and maps to 1015 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000356443.9MYOM1-20257071685aaENSP00000348821.4
 
Protein coding
CCDS45824P52179-1 NM_003803.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000261606.11MYOM1-20151541589aaENSP00000261606.7
 
Protein coding
CCDS45823P52179-2 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000581075.1MYOM1-204684121aaENSP00000462039.1
 
Nonsense mediated decay
J3KRK2 -TSL:5CDS 5' incomplete
ENST00000581804.1MYOM1-205545No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000577294.1MYOM1-203754No protein-
 
Retained intron
--TSL:2
ENST00000582016.1MYOM1-206571No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 38, Coding exons: 37, Transcript length: 5,707 bps, Translation length: 1,685 residues

MANE

This MANE Select transcript contains ENSP00000348821 and matches to NM_003803.4 and NP_003794.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: P52179

CCDS

This transcript is a member of the Human CCDS set: CCDS45824

Transcript Support Level (TSL)

TSL:1

Version

ENST00000356443.9

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.